14-37969092-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969092
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969092
    reference: chr 14
allele count: 90
allele frequency: 1.649923003593166e-3
allele num: 54548
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1032-21T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.489-21T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.496-21T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.939-21T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1032-21T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.939-21T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.939-21T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1032-21T>A
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 1.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8128
  bin: 1.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27364
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15065
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1464
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3270
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4408
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 14651
  bin: 6.25e1
  variant carriers: 3
num of homozygotes: 2
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-37969099-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969099
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969099
    reference: chr 14
allele count: 32
allele frequency: 4.626416840157298e-4
allele num: 69168
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1032-14T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.489-14T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.496-14T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.939-14T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1032-14T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.939-14T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1032-14T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.939-14T>A
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24291
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23211
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 9.75e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

14-37969101-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969101
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969101
    reference: chr 14
allele count: 1
allele frequency: 1.331416094157746e-5
allele num: 75108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.939-12A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1032-12A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.939-12A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.939-12A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.489-12A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1032-12A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.496-12A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1032-12A>G
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27791
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20878
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1758
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28175
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

14-37969103-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969103
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969103
    reference: chr 14
allele count: 2
allele frequency: 2.436290990595917e-5
allele num: 82092
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.939-10A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.939-10A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.939-10A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1032-10A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1032-10A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1032-10A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.489-10A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.496-10A>G
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18078
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ

14-37969109-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969109
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969109
    reference: chr 14
allele count: 3
allele frequency: 2.998081228014071e-5
allele num: 100064
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.496-4T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1032-4T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.939-4T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.939-4T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1032-4T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1032-4T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.489-4T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.939-4T>C
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2222
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
hgvs: c.1032-4T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

14-37969112-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969112
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969112
    reference: chr 14
allele count: 1
allele frequency: 9.382623381497466e-6
allele num: 106580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1032-1G>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.939-1G>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.489-1G>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.939-1G>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1032-1G>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.496-1G>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.939-1G>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1032-1G>T
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47053
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2447
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6815
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1032-1G>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

14-37969114-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969114
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969114
    reference: chr 14
allele count: 1
allele frequency: 9.155329317195539e-6
allele num: 109226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.940T>G
  hgvsp: ENSP00000450479.1:p.Leu314Val
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.940T>G
  hgvsp: ENSP00000438319.2:p.Leu314Val
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.490T>G
  hgvsp: ENSP00000437891.1:p.Leu164Val
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1033T>G
  hgvsp: ENSP00000444254.1:p.Leu345Val
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.497T>G
  hgvsp: ENSP00000452478.1:p.Phe166Cys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.940T>G
  hgvsp: ENSP00000442529.1:p.Leu314Val
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1033T>G
  hgvsp: ENSP00000379589.2:p.Leu345Val
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1033T>G
  hgvsp: ENSP00000333539.7:p.Leu345Val
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5588
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu345Val
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/14-37969133-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969133
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969133
    reference: chr 14
allele count: 1
allele frequency: 8.510928031592565e-6
allele num: 117496
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1052A>C
  hgvsp: ENSP00000333539.7:p.Gln351Pro
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.959A>C
  hgvsp: ENSP00000450479.1:p.Gln320Pro
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1052A>C
  hgvsp: ENSP00000379589.2:p.Gln351Pro
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.516A>C
  hgvsp: ENST00000555870.1:c.516A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.509A>C
  hgvsp: ENSP00000437891.1:p.Gln170Pro
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1052A>C
  hgvsp: ENSP00000444254.1:p.Gln351Pro
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.959A>C
  hgvsp: ENSP00000438319.2:p.Gln320Pro
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.959A>C
  hgvsp: ENSP00000442529.1:p.Gln320Pro
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln351Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

14-37969134-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969134
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969134
    reference: chr 14
allele count: 1
allele frequency: 8.494156020657787e-6
allele num: 117728
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1053A>G
  hgvsp: ENST00000327441.7:c.1053A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.960A>G
  hgvsp: ENST00000545536.1:c.960A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1053A>G
  hgvsp: ENST00000396294.2:c.1053A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.960A>G
  hgvsp: ENST00000539062.2:c.960A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.960A>G
  hgvsp: ENST00000556451.1:c.960A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.517A>G
  hgvsp: ENSP00000452478.1:p.Arg173Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.510A>G
  hgvsp: ENST00000536774.1:c.510A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1053A>G
  hgvsp: ENST00000537471.1:c.1053A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1667
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53311
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg173Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

14-37969138-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969138
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969138
    reference: chr 14
allele count: 1
allele frequency: 8.448657508321927e-6
allele num: 118362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.964G>A
  hgvsp: ENSP00000450479.1:p.Glu322Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.514G>A
  hgvsp: ENSP00000437891.1:p.Glu172Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.521G>A
  hgvsp: ENSP00000452478.1:p.Arg174Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1057G>A
  hgvsp: ENSP00000444254.1:p.Glu353Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.964G>A
  hgvsp: ENSP00000438319.2:p.Glu322Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1057G>A
  hgvsp: ENSP00000333539.7:p.Glu353Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1057G>A
  hgvsp: ENSP00000379589.2:p.Glu353Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.964G>A
  hgvsp: ENSP00000442529.1:p.Glu322Lys
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu353Lys
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: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

14-37969147-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969147
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969147
    reference: chr 14
allele count: 1
allele frequency: 8.376752835530836e-6
allele num: 119378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.523A>G
  hgvsp: ENSP00000437891.1:p.Lys175Glu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.973A>G
  hgvsp: ENSP00000442529.1:p.Lys325Glu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.973A>G
  hgvsp: ENSP00000450479.1:p.Lys325Glu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1066A>G
  hgvsp: ENSP00000379589.2:p.Lys356Glu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.973A>G
  hgvsp: ENSP00000438319.2:p.Lys325Glu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.530A>G
  hgvsp: ENSP00000452478.1:p.Glu177Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1066A>G
  hgvsp: ENSP00000444254.1:p.Lys356Glu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1066A>G
  hgvsp: ENSP00000333539.7:p.Lys356Glu
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 947
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54214
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys356Glu
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

14-37969155-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969155
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969155
    reference: chr 14
allele count: 1
allele frequency: 8.328891257995735e-6
allele num: 120064
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1074G>C
  hgvsp: ENSP00000333539.7:p.Gln358His
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.538G>C
  hgvsp: ENSP00000452478.1:p.Val180Leu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1074G>C
  hgvsp: ENSP00000444254.1:p.Gln358His
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.981G>C
  hgvsp: ENSP00000450479.1:p.Gln327His
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.981G>C
  hgvsp: ENSP00000438319.2:p.Gln327His
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1074G>C
  hgvsp: ENSP00000379589.2:p.Gln358His
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.531G>C
  hgvsp: ENSP00000437891.1:p.Gln177His
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.981G>C
  hgvsp: ENSP00000442529.1:p.Gln327His
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln358His
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

14-37969156-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969156
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969156
    reference: chr 14
allele count: 2
allele frequency: 1.665278934221482e-5
allele num: 120100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.982T>C
  hgvsp: ENSP00000438319.2:p.Phe328Leu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1075T>C
  hgvsp: ENSP00000379589.2:p.Phe359Leu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.532T>C
  hgvsp: ENSP00000437891.1:p.Phe178Leu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1075T>C
  hgvsp: ENSP00000333539.7:p.Phe359Leu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.539T>C
  hgvsp: ENSP00000452478.1:p.Val180Ala
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.982T>C
  hgvsp: ENSP00000450479.1:p.Phe328Leu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.982T>C
  hgvsp: ENSP00000442529.1:p.Phe328Leu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1075T>C
  hgvsp: ENSP00000444254.1:p.Phe359Leu
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Phe359Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

14-37969160-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969160
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969160
    reference: chr 14
allele count: 1
allele frequency: 8.311999202048076e-6
allele num: 120308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1079A>G
  hgvsp: ENSP00000444254.1:p.Asn360Ser
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.543A>G
  hgvsp: ENST00000555870.1:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.986A>G
  hgvsp: ENSP00000450479.1:p.Asn329Ser
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.986A>G
  hgvsp: ENSP00000438319.2:p.Asn329Ser
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1079A>G
  hgvsp: ENSP00000379589.2:p.Asn360Ser
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.986A>G
  hgvsp: ENSP00000442529.1:p.Asn329Ser
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.536A>G
  hgvsp: ENSP00000437891.1:p.Asn179Ser
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1079A>G
  hgvsp: ENSP00000333539.7:p.Asn360Ser
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asn360Ser
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-37969163-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969163
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969163
    reference: chr 14
allele count: 1
allele frequency: 8.302751531857658e-6
allele num: 120442
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.989A>G
  hgvsp: ENSP00000450479.1:p.Tyr330Cys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*3A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.989A>G
  hgvsp: ENSP00000438319.2:p.Tyr330Cys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1082A>G
  hgvsp: ENSP00000444254.1:p.Tyr361Cys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.539A>G
  hgvsp: ENSP00000437891.1:p.Tyr180Cys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1082A>G
  hgvsp: ENSP00000333539.7:p.Tyr361Cys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.989A>G
  hgvsp: ENSP00000442529.1:p.Tyr330Cys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1082A>G
  hgvsp: ENSP00000379589.2:p.Tyr361Cys
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Tyr361Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/14-37969166-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969166
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969166
    reference: chr 14
allele count: 2
allele frequency: 1.65953068472236e-5
allele num: 120516
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1085C>A
  hgvsp: ENSP00000333539.7:p.Thr362Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*6C>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1085C>A
  hgvsp: ENSP00000444254.1:p.Thr362Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1085C>A
  hgvsp: ENSP00000379589.2:p.Thr362Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.992C>A
  hgvsp: ENSP00000442529.1:p.Thr331Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.992C>A
  hgvsp: ENSP00000438319.2:p.Thr331Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.992C>A
  hgvsp: ENSP00000450479.1:p.Thr331Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.542C>A
  hgvsp: ENSP00000437891.1:p.Thr181Asn
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3034
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr362Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

14-37969166-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969166
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969166
    reference: chr 14
allele count: 1
allele frequency: 8.297653423611802e-6
allele num: 120516
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1085C>T
  hgvsp: ENSP00000379589.2:p.Thr362Ile
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1085C>T
  hgvsp: ENSP00000444254.1:p.Thr362Ile
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.992C>T
  hgvsp: ENSP00000438319.2:p.Thr331Ile
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.992C>T
  hgvsp: ENSP00000442529.1:p.Thr331Ile
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.542C>T
  hgvsp: ENSP00000437891.1:p.Thr181Ile
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.992C>T
  hgvsp: ENSP00000450479.1:p.Thr331Ile
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1085C>T
  hgvsp: ENSP00000333539.7:p.Thr362Ile
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*6C>T
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54776
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr362Ile
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

14-37969172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969172
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969172
    reference: chr 14
allele count: 3
allele frequency: 2.485707183693761e-5
allele num: 120690
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.998G>A
  hgvsp: ENSP00000438319.2:p.Ser333Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*12G>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.998G>A
  hgvsp: ENSP00000442529.1:p.Ser333Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1091G>A
  hgvsp: ENSP00000444254.1:p.Ser364Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.998G>A
  hgvsp: ENSP00000450479.1:p.Ser333Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.548G>A
  hgvsp: ENSP00000437891.1:p.Ser183Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1091G>A
  hgvsp: ENSP00000333539.7:p.Ser364Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1091G>A
  hgvsp: ENSP00000379589.2:p.Ser364Asn
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser364Asn
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/14-37969176-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969176
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969176
    reference: chr 14
allele count: 4
allele frequency: 3.311313101210285e-5
allele num: 120798
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1095A>C
  hgvsp: ENST00000396294.2:c.1095A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1095A>C
  hgvsp: ENST00000537471.1:c.1095A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1002A>C
  hgvsp: ENST00000545536.1:c.1002A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1095A>C
  hgvsp: ENST00000327441.7:c.1095A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*16A>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.552A>C
  hgvsp: ENST00000536774.1:c.552A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1002A>C
  hgvsp: ENST00000556451.1:c.1002A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1002A>C
  hgvsp: ENST00000539062.2:c.1002A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr365Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/14-37969182-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969182
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969182
    reference: chr 14
allele count: 1
allele frequency: 8.271298593879239e-6
allele num: 120900
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.558A>C
  hgvsp: ENSP00000437891.1:p.Glu186Asp
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1008A>C
  hgvsp: ENSP00000438319.2:p.Glu336Asp
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1101A>C
  hgvsp: ENSP00000379589.2:p.Glu367Asp
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1101A>C
  hgvsp: ENSP00000333539.7:p.Glu367Asp
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1008A>C
  hgvsp: ENSP00000450479.1:p.Glu336Asp
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1101A>C
  hgvsp: ENSP00000444254.1:p.Glu367Asp
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1008A>C
  hgvsp: ENSP00000442529.1:p.Glu336Asp
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*22A>C
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu367Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

14-37969186-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969186
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969186
    reference: chr 14
allele count: 2
allele frequency: 1.653329806229747e-5
allele num: 120968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1012G>A
  hgvsp: ENSP00000438319.2:p.Ala338Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1105G>A
  hgvsp: ENSP00000444254.1:p.Ala369Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.562G>A
  hgvsp: ENSP00000437891.1:p.Ala188Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1105G>A
  hgvsp: ENSP00000379589.2:p.Ala369Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1105G>A
  hgvsp: ENSP00000333539.7:p.Ala369Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1012G>A
  hgvsp: ENSP00000450479.1:p.Ala338Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*26G>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1012G>A
  hgvsp: ENSP00000442529.1:p.Ala338Thr
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala369Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

14-37969188-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969188
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969188
    reference: chr 14
allele count: 1
allele frequency: 8.266239026567692e-6
allele num: 120974
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1107T>C
  hgvsp: ENST00000537471.1:c.1107T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*28T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1107T>C
  hgvsp: ENST00000327441.7:c.1107T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1014T>C
  hgvsp: ENST00000556451.1:c.1014T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1107T>C
  hgvsp: ENST00000396294.2:c.1107T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1014T>C
  hgvsp: ENST00000539062.2:c.1014T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.564T>C
  hgvsp: ENST00000536774.1:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1014T>C
  hgvsp: ENST00000545536.1:c.1014T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala369Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

14-37969191-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969191
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969191
    reference: chr 14
allele count: 1
allele frequency: 8.264736024331383e-6
allele num: 120996
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1017A>T
  hgvsp: ENSP00000450479.1:p.Leu339Phe
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1110A>T
  hgvsp: ENSP00000379589.2:p.Leu370Phe
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1110A>T
  hgvsp: ENSP00000333539.7:p.Leu370Phe
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1017A>T
  hgvsp: ENSP00000438319.2:p.Leu339Phe
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1017A>T
  hgvsp: ENSP00000442529.1:p.Leu339Phe
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.567A>T
  hgvsp: ENSP00000437891.1:p.Leu189Phe
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*31A>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1110A>T
  hgvsp: ENSP00000444254.1:p.Leu370Phe
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu370Phe
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP

14-37969197-CAGAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969197
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969193
    reference: chr 14
allele count: 14
allele frequency: 1.156814463485978e-4
allele num: 121022
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1120_1123delGAGA
  hgvsp: ENSP00000379589.2:p.Glu374ThrfsTer21
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1120_1123delGAGA
  hgvsp: ENSP00000444254.1:p.Glu374ThrfsTer21
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*41_*44delGAGA
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1027_1030delGAGA
  hgvsp: ENSP00000442529.1:p.Glu343ThrfsTer21
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1027_1030delGAGA
  hgvsp: ENSP00000438319.2:p.Glu343ThrfsTer21
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1120_1123delGAGA
  hgvsp: ENSP00000333539.7:p.Glu374ThrfsTer21
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1027_1030delGAGA
  hgvsp: ENSP00000450479.1:p.Glu343ThrfsTer21
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.577_580delGAGA
  hgvsp: ENSP00000437891.1:p.Glu193ThrfsTer21
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu374ThrfsTer21
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: CAGAG
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

14-37969199-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969199
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969199
    reference: chr 14
allele count: 1
allele frequency: 8.262277744728666e-6
allele num: 121032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.575G>A
  hgvsp: ENSP00000437891.1:p.Arg192Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1025G>A
  hgvsp: ENSP00000450479.1:p.Arg342Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1118G>A
  hgvsp: ENSP00000444254.1:p.Arg373Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*39G>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1118G>A
  hgvsp: ENSP00000333539.7:p.Arg373Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1025G>A
  hgvsp: ENSP00000438319.2:p.Arg342Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1118G>A
  hgvsp: ENSP00000379589.2:p.Arg373Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1025G>A
  hgvsp: ENSP00000442529.1:p.Arg342Lys
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3048
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55055
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg373Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

14-37969201-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969201
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969201
    reference: chr 14
allele count: 1
allele frequency: 8.26255081468751e-6
allele num: 121028
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.577G>C
  hgvsp: ENSP00000437891.1:p.Glu193Gln
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1027G>C
  hgvsp: ENSP00000442529.1:p.Glu343Gln
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1027G>C
  hgvsp: ENSP00000438319.2:p.Glu343Gln
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1027G>C
  hgvsp: ENSP00000450479.1:p.Glu343Gln
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1120G>C
  hgvsp: ENSP00000444254.1:p.Glu374Gln
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*41G>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1120G>C
  hgvsp: ENSP00000333539.7:p.Glu374Gln
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1120G>C
  hgvsp: ENSP00000379589.2:p.Glu374Gln
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55042
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu374Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/14-37969206-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969206
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969206
    reference: chr 14
allele count: 2
allele frequency: 1.651827747402501e-5
allele num: 121078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1125C>A
  hgvsp: ENSP00000379589.2:p.Asn375Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.582C>A
  hgvsp: ENSP00000437891.1:p.Asn194Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1125C>A
  hgvsp: ENSP00000333539.7:p.Asn375Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1032C>A
  hgvsp: ENSP00000438319.2:p.Asn344Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1032C>A
  hgvsp: ENSP00000450479.1:p.Asn344Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*46C>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1125C>A
  hgvsp: ENSP00000444254.1:p.Asn375Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1032C>A
  hgvsp: ENSP00000442529.1:p.Asn344Lys
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3053
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn375Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-37969208-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969208
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969208
    reference: chr 14
allele count: 1
allele frequency: 8.258865892535638e-6
allele num: 121082
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*48T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.584T>C
  hgvsp: ENSP00000437891.1:p.Ile195Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1034T>C
  hgvsp: ENSP00000450479.1:p.Ile345Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1034T>C
  hgvsp: ENSP00000438319.2:p.Ile345Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1127T>C
  hgvsp: ENSP00000333539.7:p.Ile376Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1127T>C
  hgvsp: ENSP00000379589.2:p.Ile376Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1127T>C
  hgvsp: ENSP00000444254.1:p.Ile376Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1034T>C
  hgvsp: ENSP00000442529.1:p.Ile345Thr
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile376Thr
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

14-37969220-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969220
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969220
    reference: chr 14
allele count: 1
allele frequency: 8.259820927082301e-6
allele num: 121068
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1139C>G
  hgvsp: ENSP00000444254.1:p.Thr380Ser
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1139C>G
  hgvsp: ENSP00000333539.7:p.Thr380Ser
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1046C>G
  hgvsp: ENSP00000450479.1:p.Thr349Ser
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1046C>G
  hgvsp: ENSP00000438319.2:p.Thr349Ser
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1139C>G
  hgvsp: ENSP00000379589.2:p.Thr380Ser
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*60C>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.596C>G
  hgvsp: ENSP00000437891.1:p.Thr199Ser
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1046C>G
  hgvsp: ENSP00000442529.1:p.Thr349Ser
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr380Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/14-37969225-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969225
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969225
    reference: chr 14
allele count: 2
allele frequency: 1.652100645971353e-5
allele num: 121058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1144C>A
  hgvsp: ENSP00000444254.1:p.Gln382Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1051C>A
  hgvsp: ENSP00000442529.1:p.Gln351Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1051C>A
  hgvsp: ENSP00000450479.1:p.Gln351Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.601C>A
  hgvsp: ENSP00000437891.1:p.Gln201Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1144C>A
  hgvsp: ENSP00000333539.7:p.Gln382Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1144C>A
  hgvsp: ENSP00000379589.2:p.Gln382Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*65C>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1051C>A
  hgvsp: ENSP00000438319.2:p.Gln351Lys
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3044
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln382Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

14-37969225-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969225
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969225
    reference: chr 14
allele count: 2
allele frequency: 1.652100645971353e-5
allele num: 121058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1144C>T
  hgvsp: ENSP00000379589.2:p.Gln382Ter
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.601C>T
  hgvsp: ENSP00000437891.1:p.Gln201Ter
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1051C>T
  hgvsp: ENSP00000450479.1:p.Gln351Ter
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1144C>T
  hgvsp: ENSP00000333539.7:p.Gln382Ter
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1144C>T
  hgvsp: ENSP00000444254.1:p.Gln382Ter
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1051C>T
  hgvsp: ENSP00000442529.1:p.Gln351Ter
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1051C>T
  hgvsp: ENSP00000438319.2:p.Gln351Ter
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*65C>T
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55025
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln382Ter
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/14-37969247-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969247
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969247
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 120988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1073C>A
  hgvsp: ENSP00000438319.2:p.Thr358Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1073C>A
  hgvsp: ENSP00000450479.1:p.Thr358Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1166C>A
  hgvsp: ENSP00000379589.2:p.Thr389Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*87C>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1073C>A
  hgvsp: ENSP00000442529.1:p.Thr358Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1166C>A
  hgvsp: ENSP00000333539.7:p.Thr389Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.623C>A
  hgvsp: ENSP00000437891.1:p.Thr208Asn
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1166C>A
  hgvsp: ENSP00000444254.1:p.Thr389Asn
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3042
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Thr389Asn
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-37969271-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969271
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969271
    reference: chr 14
allele count: 3
allele frequency: 2.483279253029601e-5
allele num: 120808
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*111A>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.647A>C
  hgvsp: ENSP00000437891.1:p.Glu216Ala
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1190A>C
  hgvsp: ENSP00000333539.7:p.Glu397Ala
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1097A>C
  hgvsp: ENSP00000438319.2:p.Glu366Ala
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1190A>C
  hgvsp: ENSP00000379589.2:p.Glu397Ala
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1097A>C
  hgvsp: ENSP00000450479.1:p.Glu366Ala
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1097A>C
  hgvsp: ENSP00000442529.1:p.Glu366Ala
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1190A>C
  hgvsp: ENSP00000444254.1:p.Glu397Ala
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54809
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu397Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: MQ

14-37969274-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969274
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969274
    reference: chr 14
allele count: 5
allele frequency: 4.140443855581318e-5
allele num: 120760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1100G>A
  hgvsp: ENSP00000438319.2:p.Arg367Gln
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.650G>A
  hgvsp: ENSP00000437891.1:p.Arg217Gln
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1100G>A
  hgvsp: ENSP00000450479.1:p.Arg367Gln
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1193G>A
  hgvsp: ENSP00000379589.2:p.Arg398Gln
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1193G>A
  hgvsp: ENSP00000444254.1:p.Arg398Gln
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1193G>A
  hgvsp: ENSP00000333539.7:p.Arg398Gln
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1100G>A
  hgvsp: ENSP00000442529.1:p.Arg367Gln
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*114G>A
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg398Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

14-37969277-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969277
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969277
    reference: chr 14
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1196C>G
  hgvsp: ENSP00000379589.2:p.Ala399Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1196C>G
  hgvsp: ENSP00000444254.1:p.Ala399Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*117C>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1103C>G
  hgvsp: ENSP00000450479.1:p.Ala368Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.653C>G
  hgvsp: ENSP00000437891.1:p.Ala218Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1103C>G
  hgvsp: ENSP00000438319.2:p.Ala368Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1196C>G
  hgvsp: ENSP00000333539.7:p.Ala399Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1103C>G
  hgvsp: ENSP00000442529.1:p.Ala368Gly
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3030
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala399Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

14-37969287-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969287
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969287
    reference: chr 14
allele count: 2
allele frequency: 1.657879903179814e-5
allele num: 120636
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1113A>G
  hgvsp: ENST00000556451.1:c.1113A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1113A>G
  hgvsp: ENST00000545536.1:c.1113A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.663A>G
  hgvsp: ENST00000536774.1:c.663A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1206A>G
  hgvsp: ENST00000537471.1:c.1206A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1113A>G
  hgvsp: ENST00000539062.2:c.1113A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1206A>G
  hgvsp: ENST00000396294.2:c.1206A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1206A>G
  hgvsp: ENST00000327441.7:c.1206A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*127A>G
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Glu402Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/14-37969299-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969299
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969299
    reference: chr 14
allele count: 1
allele frequency: 8.302751531857658e-6
allele num: 120442
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1218A>C
  hgvsp: ENSP00000333539.7:p.Gln406His
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1125A>C
  hgvsp: ENSP00000442529.1:p.Gln375His
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1218A>C
  hgvsp: ENSP00000379589.2:p.Gln406His
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1125A>C
  hgvsp: ENSP00000450479.1:p.Gln375His
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1125A>C
  hgvsp: ENSP00000438319.2:p.Gln375His
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*139A>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.675A>C
  hgvsp: ENSP00000437891.1:p.Gln225His
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1218A>C
  hgvsp: ENSP00000444254.1:p.Gln406His
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln406His
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

14-37969299-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969299
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969299
    reference: chr 14
allele count: 5
allele frequency: 4.151375765928829e-5
allele num: 120442
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1125A>G
  hgvsp: ENST00000539062.2:c.1125A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1218A>G
  hgvsp: ENST00000327441.7:c.1218A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1218A>G
  hgvsp: ENST00000537471.1:c.1218A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1125A>G
  hgvsp: ENST00000556451.1:c.1125A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1218A>G
  hgvsp: ENST00000396294.2:c.1218A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*139A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1125A>G
  hgvsp: ENST00000545536.1:c.1125A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.675A>G
  hgvsp: ENST00000536774.1:c.675A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln406Gln
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-37969309-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969309
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969309
    reference: chr 14
allele count: 2
allele frequency: 1.664059639897494e-5
allele num: 120188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1135G>A
  hgvsp: ENSP00000438319.2:p.Glu379Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1228G>A
  hgvsp: ENSP00000379589.2:p.Glu410Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1135G>A
  hgvsp: ENSP00000442529.1:p.Glu379Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1228G>A
  hgvsp: ENSP00000333539.7:p.Glu410Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1228G>A
  hgvsp: ENSP00000444254.1:p.Glu410Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*149G>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1135G>A
  hgvsp: ENSP00000450479.1:p.Glu379Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.685G>A
  hgvsp: ENSP00000437891.1:p.Glu229Lys
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2997
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu410Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

14-37969311-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969311
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969311
    reference: chr 14
allele count: 1
allele frequency: 8.327226700419692e-6
allele num: 120088
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1137G>T
  hgvsp: ENSP00000438319.2:p.Glu379Asp
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1137G>T
  hgvsp: ENSP00000450479.1:p.Glu379Asp
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1230G>T
  hgvsp: ENSP00000379589.2:p.Glu410Asp
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1230G>T
  hgvsp: ENSP00000333539.7:p.Glu410Asp
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1230G>T
  hgvsp: ENSP00000444254.1:p.Glu410Asp
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1137G>T
  hgvsp: ENSP00000442529.1:p.Glu379Asp
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*151G>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.687G>T
  hgvsp: ENSP00000437891.1:p.Glu229Asp
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2993
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu410Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

14-37969313-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969313
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969313
    reference: chr 14
allele count: 1
allele frequency: 8.332361224523806e-6
allele num: 120014
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1139C>G
  hgvsp: ENSP00000442529.1:p.Ala380Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1139C>G
  hgvsp: ENSP00000438319.2:p.Ala380Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1232C>G
  hgvsp: ENSP00000333539.7:p.Ala411Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1232C>G
  hgvsp: ENSP00000379589.2:p.Ala411Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.689C>G
  hgvsp: ENSP00000437891.1:p.Ala230Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1139C>G
  hgvsp: ENSP00000450479.1:p.Ala380Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1232C>G
  hgvsp: ENSP00000444254.1:p.Ala411Gly
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*153C>G
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala411Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

14-37969320-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969320
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969320
    reference: chr 14
allele count: 3
allele frequency: 2.511637252603731e-5
allele num: 119444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1239A>G
  hgvsp: ENST00000537471.1:c.1239A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1239A>G
  hgvsp: ENST00000396294.2:c.1239A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1146A>G
  hgvsp: ENST00000556451.1:c.1146A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1239A>G
  hgvsp: ENST00000327441.7:c.1239A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.696A>G
  hgvsp: ENST00000536774.1:c.696A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1146A>G
  hgvsp: ENST00000539062.2:c.1146A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*160A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1146A>G
  hgvsp: ENST00000545536.1:c.1146A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53497
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln413Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

14-37969332-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969332
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969332
    reference: chr 14
allele count: 2
allele frequency: 1.710542070782231e-5
allele num: 116922
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*172A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1251A>G
  hgvsp: ENST00000396294.2:c.1251A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1251A>G
  hgvsp: ENST00000327441.7:c.1251A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1158A>G
  hgvsp: ENST00000545536.1:c.1158A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1158A>G
  hgvsp: ENST00000539062.2:c.1158A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1158A>G
  hgvsp: ENST00000556451.1:c.1158A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.708A>G
  hgvsp: ENST00000536774.1:c.708A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1251A>G
  hgvsp: ENST00000537471.1:c.1251A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3781
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49554
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu417Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-37969339-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969339
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969338
    reference: chr 14
allele count: 1
allele frequency: 8.632149577887885e-6
allele num: 115846
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*183delA
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.719delA
  hgvsp: ENSP00000437891.1:p.Lys240SerfsTer9
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1169delA
  hgvsp: ENSP00000438319.2:p.Lys390SerfsTer9
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1169delA
  hgvsp: ENSP00000450479.1:p.Lys390AsnfsTer20
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1262delA
  hgvsp: ENSP00000379589.2:p.Lys421SerfsTer9
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1262delA
  hgvsp: ENSP00000444254.1:p.Lys421SerfsTer9
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1262delA
  hgvsp: ENSP00000333539.7:p.Lys421SerfsTer9
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1169delA
  hgvsp: ENSP00000442529.1:p.Lys390AsnfsTer20
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48554
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4743
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys421SerfsTer9
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: CA
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

14-37969341-AAAGT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969341
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969337
    reference: chr 14
allele count: 1
allele frequency: 8.751509635412108e-6
allele num: 114266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1169+3_1169+6delAAGT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*183+3_*183+6delAAGT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1262+3_1262+6delAAGT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1169+3_1169+6delAAGT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1169+3_1169+6delAAGT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1262+3_1262+6delAAGT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.719+3_719+6delAAGT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1262+3_1262+6delAAGT
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: splice donor
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 6594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6692
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
hgvs: c.1262+3_1262+6delAAGT
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: AAAGT
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

14-37969346-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969346
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969346
    reference: chr 14
allele count: 4
allele frequency: 3.53544281421248e-5
allele num: 113140
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1262+3A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1169+3A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1169+3A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*183+3A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.719+3A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1169+3A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1262+3A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1262+3A>G
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6077
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40207
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1262+3A>G
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

14-37969356-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969356
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969356
    reference: chr 14
allele count: 1
allele frequency: 9.181387491277682e-6
allele num: 108916
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1262+13A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1262+13A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1262+13A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.719+13A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1169+13A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1169+13A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*183+13A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1169+13A>G
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2280
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

14-37969357-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969357
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969357
    reference: chr 14
allele count: 1
allele frequency: 9.182905103858657e-6
allele num: 108898
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1169+14T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*183+14T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1169+14T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1262+14T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.719+14T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1169+14T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1262+14T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1262+14T>C
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2433
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS

14-37969367-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969367
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969367
    reference: chr 14
allele count: 1
allele frequency: 9.530526275660943e-6
allele num: 104926
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1262+24A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1169+24A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1169+24A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1169+24A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1262+24A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.719+24A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*183+24A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1262+24A>G
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6482
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16794
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25768
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4034
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-37969371-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969371
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969371
    reference: chr 14
allele count: 1
allele frequency: 9.651205435558901e-6
allele num: 103614
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1169+28T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1169+28T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1169+28T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1262+28T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.719+28T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*183+28T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1262+28T>A
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1262+28T>A
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6919
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19008
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4934
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20269
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2966
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

14-37969377-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969377
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969377
    reference: chr 14
allele count: 1
allele frequency: 1.005025125628141e-5
allele num: 99500
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1262+34C>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1262+34C>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*183+34C>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1262+34C>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.719+34C>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1169+34C>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1169+34C>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1169+34C>G
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7958
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13085
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11015
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7728
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2662
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5405
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-37969378-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969378
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969378
    reference: chr 14
allele count: 1
allele frequency: 1.008308461724611e-5
allele num: 99176
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1169+35A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1262+35A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1169+35A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*183+35A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1262+35A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1169+35A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1262+35A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.719+35A>G
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12505
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17473
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1388
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13179
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5500
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7929
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2733
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum

14-37969386-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37969386
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37969386
    reference: chr 14
allele count: 1
allele frequency: 1.080730573867935e-5
allele num: 92530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.719+43C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1169+43C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1262+43C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1169+43C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1262+43C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1262+43C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1169+43C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000452478
  ensembl transcript: ENST00000555870
  gene symbol: MIPOL1
  hgvsc: ENST00000555870.1:c.*183+43C>T
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10977
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14999
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6253
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2624
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2337
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8275
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3441
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

14-37992663-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37992663
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37992664
    reference: chr 14
allele count: 9
allele frequency: 4.5e-3
allele num: 2000
alternate allele: GT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1262+23330dupT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1170-5dupT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1262+23330dupT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.719+23330dupT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1169+23330dupT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1262+23330dupT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1170-5dupT
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 7.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4258
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 3271
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

14-37992663-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37992663
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37992662
    reference: chr 14
allele count: 3
allele frequency: 1.5e-3
allele num: 2000
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1262+23330delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1262+23330delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1169+23330delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1170-5delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1170-5delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.719+23330delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1262+23330delT
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4258
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3271
  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: GT
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

14-37992737-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37992737
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37992737
    reference: chr 14
allele count: 5
allele frequency: 1.539408866995074e-3
allele num: 3248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1229T>C
  hgvsp: ENSP00000450479.1:p.Met410Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-23373T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-23373T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-23373T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1229T>C
  hgvsp: ENSP00000442529.1:p.Met410Thr
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-23373T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-23373T>C
  variant of: http://identifiers.org/hgnc/21460
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2493
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3776
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met410Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-37992795-C-CTA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37992795
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 37992797
    reference: chr 14
allele count: 25
allele frequency: 8.567511994516792e-3
allele num: 2918
alternate allele: CTA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-23314_1263-23313insAT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.1266+22_1266+23insAT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-23314_1263-23313insAT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.1266+22_1266+23insAT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-23314_720-23313insAT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-23314_1170-23313insAT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-23314_1263-23313insAT
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4954
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4291
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 9.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

14-38014889-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38014889
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38014889
    reference: chr 14
allele count: 235
allele frequency: 2.479426039248787e-2
allele num: 9478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.*11A>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-1221A>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.*11A>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-1221A>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-1221A>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-1221A>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-1221A>T
  variant of: http://identifiers.org/hgnc/21460
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 7.5e0
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 3.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 2.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 2.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 2.75e1
  variant carriers: 4
num of homozygotes: 6
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

14-38014928-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38014928
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38014928
    reference: chr 14
allele count: 533
allele frequency: 6.043083900226758e-2
allele num: 8820
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-1182C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-1182C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-1182C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-1182C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000442529
  ensembl transcript: ENST00000545536
  gene symbol: MIPOL1
  hgvsc: ENST00000545536.1:c.*50C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-1182C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000450479
  ensembl transcript: ENST00000556451
  gene symbol: MIPOL1
  hgvsc: ENST00000556451.1:c.*50C>T
  variant of: http://identifiers.org/hgnc/21460
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.25e1
  variant carriers: 219
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 2.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 1.75e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 2.5e0
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 7.5e0
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 2.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 3.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 8.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 6.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 3.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 2.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 9.75e1
  variant carriers: 476
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 5.25e1
  variant carriers: 5
num of homozygotes: 17
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

14-38016063-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38016063
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38016062
    reference: chr 14
allele count: 1
allele frequency: 9.349988780013463e-6
allele num: 106952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-45delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-45delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-45delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-45delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-45delT
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13921
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2972
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10873
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2691
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1473
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4711
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1236
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: AT
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

14-38016069-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38016069
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38016068
    reference: chr 14
allele count: 8
allele frequency: 7.666653888910185e-5
allele num: 104348
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-34delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-34delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-34delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-34delT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-34delT
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13736
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7206
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13222
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3539
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5765
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3358
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2710
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5527
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6407
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 901
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 922
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13177
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: CT
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

14-38016069-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38016069
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38016070
    reference: chr 14
allele count: 2
allele frequency: 1.916663472227546e-5
allele num: 104348
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-34dupT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-34dupT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-34dupT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-34dupT
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-34dupT
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7206
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1347
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6407
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5765
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3396
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 901
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5688
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3358
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 922
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5527
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

14-38016076-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38016076
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38016076
    reference: chr 14
allele count: 20
allele frequency: 1.845018450184502e-4
allele num: 108400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-34T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-34T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-34T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-34T>C
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-34T>C
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5940
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20337
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10702
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1476
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3937
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2828
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4807
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5757
  bin: 9.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 21925
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1343
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

14-38016079-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38016079
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38016079
    reference: chr 14
allele count: 2
allele frequency: 1.830496064433461e-5
allele num: 109260
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-31C>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-31C>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-31C>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-31C>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-31C>G
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23101
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2923
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6050
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2505
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1978
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24980
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4453
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5750
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

14-38016083-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38016083
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38016083
    reference: chr 14
allele count: 3
allele frequency: 2.708705780378135e-5
allele num: 110754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-27C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-27C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-27C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-27C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-27C>T
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27051
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9497
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29565
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5766
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4737
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2834
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1718
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1738
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

14-38016088-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38016088
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38016088
    reference: chr 14
allele count: 1
allele frequency: 8.851907586084802e-6
allele num: 112970
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-22C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-22C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-22C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-22C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-22C>T
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2129
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5771
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1703
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1796
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4282
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

14-38016097-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38016097
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38016097
    reference: chr 14
allele count: 1
allele frequency: 8.617866560954171e-6
allele num: 116038
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-13A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-13A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-13A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-13A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-13A>G
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1542
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2772
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 928
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

14-38016099-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38016099
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38016099
    reference: chr 14
allele count: 9980
allele frequency: 8.508243959828812e-2
allele num: 117298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-11C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-11C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-11C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-11C>T
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-11C>T
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 9.75e1
  variant carriers: 565
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 1.25e1
  variant carriers: 160
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 4.75e1
  variant carriers: 785
genotype depth: GenotypeDepth
  all individuals: 28534
  bin: 2.25e1
  variant carriers: 829
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 190
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 7.5e0
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 4.25e1
  variant carriers: 963
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 610
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 494
genotype depth: GenotypeDepth
  all individuals: 5189
  bin: 3.25e1
  variant carriers: 1245
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.75e1
  variant carriers: 476
genotype depth: GenotypeDepth
  all individuals: 11109
  bin: 2.75e1
  variant carriers: 1086
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 9.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.75e1
  variant carriers: 246
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.25e1
  variant carriers: 348
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 3.75e1
  variant carriers: 1149
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 3.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2039
  bin: 2.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 8.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 32320
  bin: 6.25e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 7.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 4.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 14130
  bin: 9.75e1
  variant carriers: 9245
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 5.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 9.25e1
  variant carriers: 36
num of homozygotes: 477
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

14-38016104-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38016104
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38016104
    reference: chr 14
allele count: 4
allele frequency: 3.381462820816285e-5
allele num: 118292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1263-6A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1170-6A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1263-6A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.720-6A>G
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1263-6A>G
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2295
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1599
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1693
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6304
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37612
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
hgvs: c.1263-6A>G
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

14-38016114-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38016114
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38016114
    reference: chr 14
allele count: 2
allele frequency: 1.678697330871244e-5
allele num: 119140
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1267G>A
  hgvsp: ENSP00000444254.1:p.Glu423Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1267G>A
  hgvsp: ENSP00000379589.2:p.Glu423Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.724G>A
  hgvsp: ENSP00000437891.1:p.Glu242Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1267G>A
  hgvsp: ENSP00000333539.7:p.Glu423Lys
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1174G>A
  hgvsp: ENSP00000438319.2:p.Glu392Lys
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6298
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1582
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5793
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2282
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu423Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

14-38016123-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38016123
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 38016123
    reference: chr 14
allele count: 1
allele frequency: 8.347942232239753e-6
allele num: 119790
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000379589
  ensembl transcript: ENST00000396294
  gene symbol: MIPOL1
  hgvsc: ENST00000396294.2:c.1276G>T
  hgvsp: ENSP00000379589.2:p.Val426Leu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000444254
  ensembl transcript: ENST00000537471
  gene symbol: MIPOL1
  hgvsc: ENST00000537471.1:c.1276G>T
  hgvsp: ENSP00000444254.1:p.Val426Leu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000333539
  ensembl transcript: ENST00000327441
  gene symbol: MIPOL1
  hgvsc: ENST00000327441.7:c.1276G>T
  hgvsp: ENSP00000333539.7:p.Val426Leu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000437891
  ensembl transcript: ENST00000536774
  gene symbol: MIPOL1
  hgvsc: ENST00000536774.1:c.733G>T
  hgvsp: ENSP00000437891.1:p.Val245Leu
  variant of: http://identifiers.org/hgnc/21460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151338
  ensembl protein: ENSP00000438319
  ensembl transcript: ENST00000539062
  gene symbol: MIPOL1
  hgvsc: ENST00000539062.2:c.1183G>T
  hgvsp: ENSP00000438319.2:p.Val395Leu
  variant of: http://identifiers.org/hgnc/21460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6297
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5875
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2278
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39233
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val426Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

14-38016126-G-A
type: Variant
allele count: 1
allele frequency: 8.337780149413021e-6
allele num: 119936
alternate allele: A
canonical: true
consequence: missense
filter: PASS
hgvs: p.Asp427Asn
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 176
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 400
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 136
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 26978
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3276
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1132
bin: 9.75e1
variant carriers: 73

GenotypeQuality
all individuals: 844
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 196
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 476
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 462
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4016
num of homozygotes: 0

African
type: Population
allele count: 84
allele frequency: 1.824500434404865e-2
allele num: 4604
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.729022273063724e-5
allele num: 29722
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 6.581112207963146e-4
allele num: 6078
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6768
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 8.17489e5

QD
type: SiteQuality
SIO_000300: 9.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

VQSLOD
type: SiteQuality
SIO_000300: 4.53e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

GenotypeQuality
all individuals: 2234
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2061
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23034
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24486
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.343580372977912e-4
allele num: 37214
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.622606871230003e-4
allele num: 7626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 634
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 6.762849413886385e-4
allele num: 8872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4920
num of homozygotes: 0

African
type: Population
allele count: 15
allele frequency: 2.682403433476395e-3
allele num: 5592
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 9.280742459396752e-4
allele num: 4310
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.53295e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.42e-1

QD
type: SiteQuality
SIO_000300: 1.34e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.388e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

GenotypeQuality
all individuals: 338
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1810
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 152
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.472310126582278e-5
allele num: 40448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4980
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5986
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5262
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

QD
type: SiteQuality
SIO_000300: 1.12e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

DP
type: SiteQuality
SIO_000300: 1.008524e6

GenotypeQuality
all individuals: 1325
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1636
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32732
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44194
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10620
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.273243919072517e-4
allele num: 8798
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.17e-1

QD
type: SiteQuality
SIO_000300: 1.292e1

DP
type: SiteQuality
SIO_000300: 1.071376e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.237e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.46e-1

FS
type: SiteQuality
SIO_000300: 5.201e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 80
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 170
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 9861
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43448
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.521607892218214e-5
allele num: 54332
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6282
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13366
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 3.305e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.224845e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.08e-1

QD
type: SiteQuality
SIO_000300: 1.696e1

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 172
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6418
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.482268158543523e-5
allele num: 10546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7752
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14478
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.01e1

DP
type: SiteQuality
SIO_000300: 1.282593e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.83e-1

GenotypeQuality
all individuals: 161
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2556
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48672
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 366
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14946
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7922
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.672856234735187e-5
allele num: 59778
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.447e-1

QD
type: SiteQuality
SIO_000300: 1.87e1

FS
type: SiteQuality
SIO_000300: 2.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.43e0

MQRankSum
type: SiteQuality
SIO_000300: 8.01e-1

DP
type: SiteQuality
SIO_000300: 1.303771e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
all individuals: 1770
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53204
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2879
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 69
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.518372304889159e-4
allele num: 6586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16262
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11206
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.346e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

QD
type: SiteQuality
SIO_000300: 1.688e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

VQSLOD
type: SiteQuality
SIO_000300: -1.995e0

DP
type: SiteQuality
SIO_000300: 1.379679e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

FS
type: SiteQuality
SIO_000300: 2.013e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 70
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541829843658454e-5
allele num: 64858
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11210
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: 8434
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e0

FS
type: SiteQuality
SIO_000300: 2.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

DP
type: SiteQuality
SIO_000300: 1.38189e6

VQSLOD
type: SiteQuality
SIO_000300: 2.6e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e-1

QD
type: SiteQuality
SIO_000300: 1.422e1

GenotypeQuality
all individuals: 2921
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53652
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 90
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.040149781568546e-4
allele num: 9614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.684e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.426e0

MQ
type: SiteQuality
SIO_000300: 5.764e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

DP
type: SiteQuality
SIO_000300: 1.387406e6

MQRankSum
type: SiteQuality
SIO_000300: -1.22e0

QD
type: SiteQuality
SIO_000300: 1.579e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

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

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2968
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9836
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.089392278650591e-5
allele num: 16422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65762
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: 8540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.081e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 1.397211e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.9e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

GenotypeQuality
all individuals: 1078
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 431
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54548
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 376
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3013
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 197
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10040
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.080505898090721e-5
allele num: 16446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66116
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.402902e6

VQSLOD
type: SiteQuality
SIO_000300: -4.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.03e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.707e0

QD
type: SiteQuality
SIO_000300: 1.516e1

GenotypeQuality
all individuals: 1078
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 54560
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3015
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.023980162690133e-5
allele num: 66138
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

MQRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.26e-1

DP
type: SiteQuality
SIO_000300: 1.403116e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

FS
type: SiteQuality
SIO_000300: 9.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.0e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 54678
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 540
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 378
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509844184080203e-5
allele num: 66232
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

FS
type: SiteQuality
SIO_000300: 9.320000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.02e0

VQSLOD
type: SiteQuality
SIO_000300: 8.62e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: -7.75e-1

DP
type: SiteQuality
SIO_000300: 1.404668e6

QD
type: SiteQuality
SIO_000300: 1.285e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3031
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54751
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10144
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

DP
type: SiteQuality
SIO_000300: 1.4058e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e0

VQSLOD
type: SiteQuality
SIO_000300: -1.44e0

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

QD
type: SiteQuality
SIO_000300: 1.218e1

MQ
type: SiteQuality
SIO_000300: 5.471e1

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54776
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 379
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507204437209863e-5
allele num: 66348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.83477576711251e-5
allele num: 10168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.488e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.82e-1

DP
type: SiteQuality
SIO_000300: 1.406864e6

QD
type: SiteQuality
SIO_000300: 1.365e1

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1079
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3034
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.83477576711251e-5
allele num: 10168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.29e0

DP
type: SiteQuality
SIO_000300: 1.406864e6

QD
type: SiteQuality
SIO_000300: 1.365e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.488e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54857
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3046
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.31858407079646e-3
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66436
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.184e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

VQSLOD
type: SiteQuality
SIO_000300: 6.81e-1

FS
type: SiteQuality
SIO_000300: 2.363e0

DP
type: SiteQuality
SIO_000300: 1.408686e6

QD
type: SiteQuality
SIO_000300: 1.265e1

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 318
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3051
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54925
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 196
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 7.25e1
variant carriers: 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: 1.504121292341014e-5
allele num: 66484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.746114894360049e-4
allele num: 11454
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.070171178827243e-5
allele num: 16474
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

FS
type: SiteQuality
SIO_000300: 5.519e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

VQSLOD
type: SiteQuality
SIO_000300: 8.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

DP
type: SiteQuality
SIO_000300: 1.409672e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.347e1

GenotypeQuality
all individuals: 54964
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3054
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

East Asian
type: Population
allele count: 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: 10292
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.410543e6

QD
type: SiteQuality
SIO_000300: 6.899999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

VQSLOD
type: SiteQuality
SIO_000300: -3.324e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

GenotypeQuality
all individuals: 235
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 9.75e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 194
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54998
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3049
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.848e0

QD
type: SiteQuality
SIO_000300: 1.197e1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: -8.9e-2

DP
type: SiteQuality
SIO_000300: 1.41123e6

GenotypeQuality
all individuals: 195
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3052
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 55019
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.689922480620155e-5
allele num: 10320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
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: 906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.128e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 8.149999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.601e1

MQRankSum
type: SiteQuality
SIO_000300: -1.314e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.37e-1

DP
type: SiteQuality
SIO_000300: 1.411311e6

VQSLOD
type: SiteQuality
SIO_000300: -1.877e-1

GenotypeQuality
all individuals: 55021
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3053
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502223290469895e-5
allele num: 66568
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

FS
type: SiteQuality
SIO_000300: 1.914e0

QD
type: SiteQuality
SIO_000300: 1.057e1

DP
type: SiteQuality
SIO_000300: 1.411509e6

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3048
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55025
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1090
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.952655611631819e-4
allele num: 66576
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

FS
type: SiteQuality
SIO_000300: 2.702e0

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.725e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.25e-1

DP
type: SiteQuality
SIO_000300: 1.412693e6

QD
type: SiteQuality
SIO_000300: 1.146e1

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1086
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.663703131039814e-5
allele num: 10348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 2.706e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.694e0

MQRankSum
type: SiteQuality
SIO_000300: -7.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.263e0

DP
type: SiteQuality
SIO_000300: 1.412832e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

VQSLOD
type: SiteQuality
SIO_000300: 3.49e-1

QD
type: SiteQuality
SIO_000300: 1.251e1

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3048
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1082
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502223290469895e-5
allele num: 66568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.41213e6

VQSLOD
type: SiteQuality
SIO_000300: 3.5e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 1.899e0

QD
type: SiteQuality
SIO_000300: 1.275e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.993e0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 193
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1079
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55013
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.738223535546671e-4
allele num: 11506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 8.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: -7.202e-1

DP
type: SiteQuality
SIO_000300: 1.412403e6

QD
type: SiteQuality
SIO_000300: 1.024e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.196e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.15e0

GenotypeQuality
all individuals: 55049
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1078
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.64e-1

FS
type: SiteQuality
SIO_000300: 3.835e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.13e-1

QD
type: SiteQuality
SIO_000300: 1.586e1

DP
type: SiteQuality
SIO_000300: 1.412478e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55024
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 195
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 456
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3046
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501726986033939e-5
allele num: 66590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
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: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.412474e6

QD
type: SiteQuality
SIO_000300: 1.208e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.44e0

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: -5.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.46e-1

FS
type: SiteQuality
SIO_000300: 1.575e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 195
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55025
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 7.75e1
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: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 8.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.412651e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 8.4e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e-1

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

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3044
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.2e0

QD
type: SiteQuality
SIO_000300: 8.4e0

DP
type: SiteQuality
SIO_000300: 1.412651e6

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 274
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54957
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 381
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
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: 16468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.42e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 1.95337e2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.4117e6

VQSLOD
type: SiteQuality
SIO_000300: -1.74e2

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.423e0

GenotypeQuality
all individuals: 196
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 416
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.481086098862845e-4
allele num: 8618
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.127e1

DP
type: SiteQuality
SIO_000300: 1.409675e6

FS
type: SiteQuality
SIO_000300: 4.05e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54734
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 92
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3032
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 9.75e1
variant carriers: 5

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.320724065908564e-4
allele num: 8618
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505933377507379e-5
allele num: 66404
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.313e1

DP
type: SiteQuality
SIO_000300: 1.409579e6

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.71e-1

FS
type: SiteQuality
SIO_000300: 2.087e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.248e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

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

GenotypeQuality
all individuals: 54751
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 92
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66390
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

FS
type: SiteQuality
SIO_000300: 2.063e0

DP
type: SiteQuality
SIO_000300: 1.409048e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.03e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.27e-1

QD
type: SiteQuality
SIO_000300: 3.162e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.183e0

GenotypeQuality
all individuals: 3027
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 443
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 92
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54660
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 380
bin: 7.75e1
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: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.750390015600624e-5
allele num: 10256
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

FS
type: SiteQuality
SIO_000300: 5.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.039e0

DP
type: SiteQuality
SIO_000300: 1.407697e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.34e-1

QD
type: SiteQuality
SIO_000300: 1.286e1

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54464
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3011
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 444
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 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: 8602
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.103515625e-5
allele num: 16384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66250
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.68e-1

QD
type: SiteQuality
SIO_000300: 1.275e1

MQRankSum
type: SiteQuality
SIO_000300: 9.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 1.062e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.76e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

DP
type: SiteQuality
SIO_000300: 1.405833e6

GenotypeQuality
all individuals: 444
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3011
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54464
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 9.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.220703125e-4
allele num: 16384
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.721437292865864e-5
allele num: 11466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.018867924528302e-5
allele num: 66250
num of homozygotes: 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: 8602
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.23e-1

QD
type: SiteQuality
SIO_000300: 1.275e1

FS
type: SiteQuality
SIO_000300: 1.062e0

DP
type: SiteQuality
SIO_000300: 1.405833e6

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.68e-1

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54266
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1079
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 188
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511761504505049e-5
allele num: 66148
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.118453255017132e-5
allele num: 16344
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.94e1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.307e0

DP
type: SiteQuality
SIO_000300: 1.403497e6

FS
type: SiteQuality
SIO_000300: 1.0836e1

QD
type: SiteQuality
SIO_000300: 9.94e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.29e0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.750437521876094e-5
allele num: 11428
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66106
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10150
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.402419e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.027e0

VQSLOD
type: SiteQuality
SIO_000300: 8.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.379e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.3e0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1079
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 374
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54055
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2990
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66070
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166044776119403e-4
allele num: 8576
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: 16296
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.089e0

MQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e0

QD
type: SiteQuality
SIO_000300: 9.81e0

VQSLOD
type: SiteQuality
SIO_000300: -2.187e-1

FS
type: SiteQuality
SIO_000300: 1.306e0

DP
type: SiteQuality
SIO_000300: 1.401991e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.952e1

GenotypeQuality
all individuals: 185
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2966
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 372
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65858
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.499766682221185e-4
allele num: 8572
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 1.395981e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.46e-1

FS
type: SiteQuality
SIO_000300: 5.158e0

MQRankSum
type: SiteQuality
SIO_000300: 6.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e-1

QD
type: SiteQuality
SIO_000300: 1.6e1

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2783
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11170
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.021835826930853e-4
allele num: 9892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64762
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15214
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.72e-1

DP
type: SiteQuality
SIO_000300: 1.364669e6

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 4.631e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.664e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.23e0

GenotypeQuality
all individuals: 206
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2750
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.556226462074761e-5
allele num: 64258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11094
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8358
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.023e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.350589e6

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.09e-1

QD
type: SiteQuality
SIO_000300: 1.238e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

GenotypeQuality
all individuals: 352
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45360
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2527
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10936
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 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: 8226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14540
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.173e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 5.381e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.41e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.642e0

DP
type: SiteQuality
SIO_000300: 1.319592e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

FS
type: SiteQuality
SIO_000300: 7.55e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

GenotypeQuality
all individuals: 297
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43374
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8162
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2492
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9650
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.802690582959641e-4
allele num: 14272
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.2e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.88e0

FS
type: SiteQuality
SIO_000300: 3.944e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.83e-1

DP
type: SiteQuality
SIO_000300: 1.293986e6

VQSLOD
type: SiteQuality
SIO_000300: 9.83e-1

GenotypeQuality
all individuals: 1066
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34778
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12853
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2435
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2137
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7784
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.645765445508706e-5
allele num: 60762
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.79e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.56e-1

QD
type: SiteQuality
SIO_000300: 7.6e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e-1

DP
type: SiteQuality
SIO_000300: 1.205534e6

GenotypeQuality
all individuals: 2129
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 324
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12897
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2284
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 403
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 178
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60748
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.545117428924598e-4
allele num: 6472
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13402
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.44e-1

DP
type: SiteQuality
SIO_000300: 1.205075e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

QD
type: SiteQuality
SIO_000300: 1.15e1

MQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

FS
type: SiteQuality
SIO_000300: 3.274e0

GenotypeQuality
all individuals: 1966
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4413
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9974
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9056
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58684
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.342642320085929e-4
allele num: 7448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.17e-1

FS
type: SiteQuality
SIO_000300: 2.863e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.51e0

MQRankSum
type: SiteQuality
SIO_000300: 3.99e-1

DP
type: SiteQuality
SIO_000300: 1.102698e6

QD
type: SiteQuality
SIO_000300: 1.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.75e-1

GenotypeQuality
all individuals: 281
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17805
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6025
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1723
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12348
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8906
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.363512407962912e-4
allele num: 7334
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57976
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.612e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.211e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.99e-1

DP
type: SiteQuality
SIO_000300: 1.048266e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.58e-1

GenotypeQuality
all individuals: 17639
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1267
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4678
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 266
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14014
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.804366966015144e-5
allele num: 11358
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7010
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55882
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.162e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.86111e5

VQSLOD
type: SiteQuality
SIO_000300: -1.477e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e0

QD
type: SiteQuality
SIO_000300: 1.494e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.303e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.936e0

GenotypeQuality
all individuals: 1160
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1027
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4924
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55654
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6986
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.919999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.752e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.794e0

QD
type: SiteQuality
SIO_000300: 1.089e1

DP
type: SiteQuality
SIO_000300: 9.77624e5

MQRankSum
type: SiteQuality
SIO_000300: -4.29e-1

GenotypeQuality
all individuals: 228
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2195
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7625
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5257
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2848
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.913362926679933e-5
allele num: 52264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9926
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8144
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.3323e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.081e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.277e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 14
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 103
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 6.75e1
variant carriers: 3

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 1.056338028169014e-2
allele num: 284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 7.263922518159807e-3
allele num: 826
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.197e0

QD
type: SiteQuality
SIO_000300: 1.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.03e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

DP
type: SiteQuality
SIO_000300: 4.9065e4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 103
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1721
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.210653753026634e-3
allele num: 826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.125e-3
allele num: 640
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.197e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

DP
type: SiteQuality
SIO_000300: 4.9065e4

QD
type: SiteQuality
SIO_000300: 1.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.03e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 60
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1124
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 2.11864406779661e-2
allele num: 236
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 84
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.83e0

DP
type: SiteQuality
SIO_000300: 6.8672e4

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.36e-2

QD
type: SiteQuality
SIO_000300: 9.960000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -4.412e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

GenotypeQuality
all individuals: 135
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1066
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1152
num of homozygotes: 0

African
type: Population
allele count: 25
allele frequency: 6.756756756756757e-2
allele num: 370
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.76e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.0768e4

VQSLOD
type: SiteQuality
SIO_000300: 5.61e0

MQ
type: SiteQuality
SIO_000300: 6.006e1

QD
type: SiteQuality
SIO_000300: 1.798e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.11e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.35e-1

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1090
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1787
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 60
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 2565
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 31
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 364
bin: 9.75e1
variant carriers: 204

GenotypeQuality
all individuals: 53
bin: 9.25e1
variant carriers: 7

GenotypeQuality
all individuals: 187
bin: 6.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 66
allele frequency: 2.396514161220044e-2
allele num: 2754
num of homozygotes: 1

South Asian
type: Population
allele count: 113
allele frequency: 1.978291316526611e-2
allele num: 5712
num of homozygotes: 1

Latino
type: Population
allele count: 14
allele frequency: 8.045977011494253e-2
allele num: 174
num of homozygotes: 0

East Asian
type: Population
allele count: 29
allele frequency: 1.510416666666667e-1
allele num: 192
num of homozygotes: 4

African
type: Population
allele count: 6
allele frequency: 1.136363636363636e-2
allele num: 528
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 6.03448275862069e-2
allele num: 116
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

FS
type: SiteQuality
SIO_000300: 5.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.21e1

VQSLOD
type: SiteQuality
SIO_000300: 4.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.16334e5

ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

GenotypeQuality
all individuals: 1353
bin: 7.5e0
variant carriers: 12

GenotypeQuality
all individuals: 557
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 235
bin: 1.25e1
variant carriers: 8

GenotypeQuality
all individuals: 478
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 13

GenotypeQuality
all individuals: 227
bin: 4.25e1
variant carriers: 6

GenotypeQuality
all individuals: 101
bin: 6.75e1
variant carriers: 8

GenotypeQuality
all individuals: 58
bin: 9.25e1
variant carriers: 16

GenotypeQuality
all individuals: 1287
bin: 2.25e1
variant carriers: 8

GenotypeQuality
all individuals: 53
bin: 7.25e1
variant carriers: 9

African
type: Population
allele count: 9
allele frequency: 1.737451737451737e-2
allele num: 518
num of homozygotes: 0

South Asian
type: Population
allele count: 335
allele frequency: 6.41025641025641e-2
allele num: 5226
num of homozygotes: 11

European (Non-Finnish)
type: Population
allele count: 169
allele frequency: 6.465187452180567e-2
allele num: 2614
num of homozygotes: 5

Other
type: Population
allele count: 7
allele frequency: 6.862745098039216e-2
allele num: 102
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 6.976744186046512e-2
allele num: 172
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 5.0e-1
allele num: 2
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

FS
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.72e0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

QD
type: SiteQuality
SIO_000300: 1.304e1

DP
type: SiteQuality
SIO_000300: 9.9629e4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.827e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 5936
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3505
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1822
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5717
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5976
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9654
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7754
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.093135111499781e-4
allele num: 9148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6008
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

DP
type: SiteQuality
SIO_000300: 1.449765e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.25e0

GenotypeQuality
all individuals: 599
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1215
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5688
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3396
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1347
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.700102006120367e-4
allele num: 5882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8994
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.902263942573165e-5
allele num: 57952
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.16076058772688e-4
allele num: 9256
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.318565400843882e-4
allele num: 7584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13904
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

FS
type: SiteQuality
SIO_000300: 3.875e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

QD
type: SiteQuality
SIO_000300: 2.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.27e-1

DP
type: SiteQuality
SIO_000300: 1.488973e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3539
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1215
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2710
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8994
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.451131971286582e-5
allele num: 57952
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.9e0

VQSLOD
type: SiteQuality
SIO_000300: -2.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

FS
type: SiteQuality
SIO_000300: 3.875e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e-1

DP
type: SiteQuality
SIO_000300: 1.488973e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 6363
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 4187
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1929
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.992296453712312e-4
allele num: 60232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6086
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.07781849536538e-4
allele num: 9278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7854
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.888268156424581e-4
allele num: 14320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

DP
type: SiteQuality
SIO_000300: 1.546691e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.356e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

MQRankSum
type: SiteQuality
SIO_000300: -1.66e-1

QD
type: SiteQuality
SIO_000300: 1.135e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.89e-1

GenotypeQuality
all individuals: 295
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4025
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14436
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.00924251557163e-4
allele num: 9954
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.715e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.933e0

DP
type: SiteQuality
SIO_000300: 1.583468e6

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 1.17e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.914e1

GenotypeQuality
all individuals: 536
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2027
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5387
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.055921052631579e-4
allele num: 14592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6196
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8084
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.48e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.708e0

DP
type: SiteQuality
SIO_000300: 1.630422e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

FS
type: SiteQuality
SIO_000300: 1.164e0

VQSLOD
type: SiteQuality
SIO_000300: 3.16e-1

QD
type: SiteQuality
SIO_000300: 1.322e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.69e0

GenotypeQuality
all individuals: 33274
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1465
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5073
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62714
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8278
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.737636437137851e-5
allele num: 14842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10418
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.211e1

VQSLOD
type: SiteQuality
SIO_000300: 5.47e-1

FS
type: SiteQuality
SIO_000300: 3.222e0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.44e-1

DP
type: SiteQuality
SIO_000300: 1.681093e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.93e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

GenotypeQuality
all individuals: 728
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36897
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5806
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2248
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64352
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.179801793298726e-4
allele num: 8476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10792
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9812
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.445e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.94e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

QD
type: SiteQuality
SIO_000300: 1.173e1

DP
type: SiteQuality
SIO_000300: 1.731193e6

GenotypeQuality
all individuals: 4339
bin: 6.75e1
variant carriers: 35

GenotypeQuality
all individuals: 1191
bin: 8.25e1
variant carriers: 30

GenotypeQuality
all individuals: 517
bin: 3.25e1
variant carriers: 8

GenotypeQuality
all individuals: 187
bin: 5.25e1
variant carriers: 15

GenotypeQuality
all individuals: 1463
bin: 7.25e1
variant carriers: 16

African
type: Population
allele count: 195
allele frequency: 1.97728655445143e-2
allele num: 9862
num of homozygotes: 4

Latino
type: Population
allele count: 371
allele frequency: 3.400549954170486e-2
allele num: 10910
num of homozygotes: 6

Other
type: Population
allele count: 93
allele frequency: 1.076388888888889e-1
allele num: 864
num of homozygotes: 4

East Asian
type: Population
allele count: 4
allele frequency: 4.706989879971758e-4
allele num: 8498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6978
allele frequency: 1.072383586906408e-1
allele num: 65070
num of homozygotes: 346

European (Finnish)
type: Population
allele count: 674
allele frequency: 1.035966799877037e-1
allele num: 6506
num of homozygotes: 30

South Asian
type: Population
allele count: 1665
allele frequency: 1.068129330254042e-1
allele num: 15588
num of homozygotes: 87

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.387e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.05e-2

MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
SIO_000300: 1.916154e6

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.423e0

VQSLOD
type: SiteQuality
SIO_000300: 5.85e0

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1007
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1890
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5736
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.338634237605239e-4
allele num: 8552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.051199121254653e-5
allele num: 65548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15758
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9964
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11046
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.913412e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-2

FS
type: SiteQuality
SIO_000300: 3.277e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

VQSLOD
type: SiteQuality
SIO_000300: 9.55e-1

QD
type: SiteQuality
SIO_000300: 1.087e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.17e-1

GenotypeQuality
all individuals: 193
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38444
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15938
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.0333363666697e-5
allele num: 65934
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10070
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 2.844e0

VQSLOD
type: SiteQuality
SIO_000300: 9.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.868e0

MQRankSum
type: SiteQuality
SIO_000300: 9.15e-1

DP
type: SiteQuality
SIO_000300: 1.926902e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.02e-1

QD
type: SiteQuality
SIO_000300: 1.334e1

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1588
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1905
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 998
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66158
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: 0
allele frequency: 0.0e0
allele num: 11286
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.204243702692642e-5
allele num: 16118
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

FS
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 1.526e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.82e-1

MQ
type: SiteQuality
SIO_000300: 5.798e1

MQRankSum
type: SiteQuality
SIO_000300: 3.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.13e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.828e0

DP
type: SiteQuality
SIO_000300: 1.935594e6