16-15810961-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810961
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810961
    reference: chr 16
allele count: 9
allele frequency: 7.424149934832462e-5
allele num: 121226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7087C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1792+36G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5504+36G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7087C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7087C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7087C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5504+36G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5525+36G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7087C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5525+36G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3424+36G>C
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22651
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

16-15810963-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810963
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810963
    reference: chr 16
allele count: 8
allele frequency: 6.599679915524098e-5
allele num: 121218
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7085T>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7085T>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1792+34A>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3424+34A>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7085T>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5525+34A>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5504+34A>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7085T>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5525+34A>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5504+34A>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7085T>C
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22651
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP

16-15810963-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810963
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810963
    reference: chr 16
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5525+34A>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5525+34A>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7085T>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5504+34A>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5504+34A>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7085T>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7085T>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7085T>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7085T>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3424+34A>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1792+34A>C
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22651
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3272
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

16-15810965-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810965
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810965
    reference: chr 16
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7083C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7083C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1792+32G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5504+32G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7083C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3424+32G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5525+32G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7083C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5504+32G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7083C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5525+32G>A
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22651
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP

16-15810969-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810969
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810969
    reference: chr 16
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7079C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5504+28G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7079C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5525+28G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7079C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7079C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1792+28G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7079C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5525+28G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3424+28G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5504+28G>A
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22651
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43804
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

16-15810972-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810972
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810972
    reference: chr 16
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3424+25C>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7076G>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5525+25C>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5504+25C>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5504+25C>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7076G>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7076G>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7076G>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7076G>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5525+25C>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1792+25C>A
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22651
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

16-15810976-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810976
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810976
    reference: chr 16
allele count: 3
allele frequency: 2.474757473767571e-5
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3424+21G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7072C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1792+21G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7072C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7072C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5525+21G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5504+21G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7072C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5504+21G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5525+21G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7072C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22651
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

16-15810978-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810978
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810978
    reference: chr 16
allele count: 2
allele frequency: 1.649811096629436e-5
allele num: 121226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7070G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7070G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5525+19C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7070G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1792+19C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7070G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3424+19C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5504+19C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5504+19C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7070G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5525+19C>T
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22652
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

16-15810978-G-GAACTCCACACCCGCAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810978
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810994
    reference: chr 16
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: GAACTCCACACCCGCAT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22652
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

16-15810989-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810989
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810989
    reference: chr 16
allele count: 201
allele frequency: 1.657896039195632e-3
allele num: 121238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7059C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5504+8G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7059C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5525+8G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7059C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5504+8G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7059C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1792+8G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7059C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3424+8G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5525+8G>C
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22734
  bin: 9.75e1
  variant carriers: 150
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: c.5525+8G>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

16-15810990-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810990
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810990
    reference: chr 16
allele count: 12
allele frequency: 9.89788680116795e-5
allele num: 121238
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5504+7G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7058C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5525+7G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3424+7G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5525+7G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1792+7G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7058C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7058C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7058C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5504+7G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7058C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22628
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
hgvs: c.5525+7G>A
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-15810990-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810990
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810990
    reference: chr 16
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5504+7G>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3424+7G>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5525+7G>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7058C>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5525+7G>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1792+7G>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5504+7G>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7058C>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7058C>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7058C>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7058C>A
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22628
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.5525+7G>T
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

16-15810991-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810991
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810991
    reference: chr 16
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7057G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7057G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5504+6C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3424+6C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5525+6C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7057G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1792+6C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5525+6C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7057G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5504+6C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7057G>A
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22626
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.5525+6C>T
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

16-15810999-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15810999
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15810999
    reference: chr 16
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7049G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5523C>G
  hgvsp: ENST00000396324.3:c.5523C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5502C>G
  hgvsp: ENST00000300036.5:c.5502C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3422C>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1790C>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5502C>G
  hgvsp: ENST00000576790.2:c.5502C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7049G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7049G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7049G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5523C>G
  hgvsp: ENST00000452625.2:c.5523C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7049G>C
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  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: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.5523C>G
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

16-15811001-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811001
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811001
    reference: chr 16
allele count: 2
allele frequency: 1.649375711293276e-5
allele num: 121258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5500G>A
  hgvsp: ENSP00000300036.5:p.Ala1834Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5521G>A
  hgvsp: ENSP00000379616.3:p.Ala1841Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5521G>A
  hgvsp: ENSP00000407821.2:p.Ala1841Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7047C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7047C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3420G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7047C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5500G>A
  hgvsp: ENSP00000458731.1:p.Ala1834Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1788G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7047C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7047C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22626
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala1841Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

16-15811002-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811002
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811002
    reference: chr 16
allele count: 37
allele frequency: 3.051395394867058e-4
allele num: 121256
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7046C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5499G>C
  hgvsp: ENSP00000458731.1:p.Glu1833Asp
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5520G>C
  hgvsp: ENSP00000407821.2:p.Glu1840Asp
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5520G>C
  hgvsp: ENSP00000379616.3:p.Glu1840Asp
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7046C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1787G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7046C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3419G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7046C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7046C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5499G>C
  hgvsp: ENSP00000300036.5:p.Glu1833Asp
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22643
  bin: 9.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu1840Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

16-15811002-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811002
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811002
    reference: chr 16
allele count: 4
allele frequency: 3.298805832288711e-5
allele num: 121256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3419G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5499G>A
  hgvsp: ENST00000300036.5:c.5499G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5499G>A
  hgvsp: ENST00000576790.2:c.5499G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7046C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5520G>A
  hgvsp: ENST00000452625.2:c.5520G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7046C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1787G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7046C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7046C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7046C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5520G>A
  hgvsp: ENST00000396324.3:c.5520G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22643
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu1840Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

16-15811005-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811005
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811005
    reference: chr 16
allele count: 13
allele frequency: 1.072076529770741e-4
allele num: 121260
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7043C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3416G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5496G>C
  hgvsp: ENSP00000300036.5:p.Gln1832His
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7043C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7043C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7043C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5517G>C
  hgvsp: ENSP00000407821.2:p.Gln1839His
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1784G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5496G>C
  hgvsp: ENSP00000458731.1:p.Gln1832His
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5517G>C
  hgvsp: ENSP00000379616.3:p.Gln1839His
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7043C>G
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22649
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1839His
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

16-15811008-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811008
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811008
    reference: chr 16
allele count: 2
allele frequency: 1.649375711293276e-5
allele num: 121258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7040C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7040C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5514G>A
  hgvsp: ENST00000396324.3:c.5514G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7040C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7040C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3413G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7040C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5493G>A
  hgvsp: ENST00000300036.5:c.5493G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1781G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5493G>A
  hgvsp: ENST00000576790.2:c.5493G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5514G>A
  hgvsp: ENST00000452625.2:c.5514G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22649
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu1838Glu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

16-15811010-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811010
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811010
    reference: chr 16
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5512G>C
  hgvsp: ENSP00000407821.2:p.Glu1838Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5491G>C
  hgvsp: ENSP00000300036.5:p.Glu1831Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7038C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7038C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1779G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7038C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3411G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5491G>C
  hgvsp: ENSP00000458731.1:p.Glu1831Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7038C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5512G>C
  hgvsp: ENSP00000379616.3:p.Glu1838Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7038C>G
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22649
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu1838Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-15811011-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811011
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811011
    reference: chr 16
allele count: 3
allele frequency: 2.474022761009401e-5
allele num: 121260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5490C>T
  hgvsp: ENST00000300036.5:c.5490C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7037G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7037G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5511C>T
  hgvsp: ENST00000452625.2:c.5511C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7037G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5490C>T
  hgvsp: ENST00000576790.2:c.5490C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7037G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5511C>T
  hgvsp: ENST00000396324.3:c.5511C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7037G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1778C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3410C>T
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22651
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val1837Val
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

16-15811013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811013
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811013
    reference: chr 16
allele count: 2
allele frequency: 1.649321304283287e-5
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7035C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7035C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3408G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5488G>A
  hgvsp: ENSP00000458731.1:p.Val1830Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5509G>A
  hgvsp: ENSP00000379616.3:p.Val1837Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1776G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5509G>A
  hgvsp: ENSP00000407821.2:p.Val1837Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7035C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5488G>A
  hgvsp: ENSP00000300036.5:p.Val1830Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7035C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7035C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22650
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val1837Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

16-15811023-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811023
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811023
    reference: chr 16
allele count: 58438
allele frequency: 4.817880521707587e-1
allele num: 121294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7025C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7025C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1766G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3398G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5499G>A
  hgvsp: ENST00000396324.3:c.5499G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5478G>A
  hgvsp: ENST00000300036.5:c.5478G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5478G>A
  hgvsp: ENST00000576790.2:c.5478G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7025C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5499G>A
  hgvsp: ENST00000452625.2:c.5499G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7025C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7025C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.25e1
  variant carriers: 233
genotype depth: GenotypeDepth
  all individuals: 6414
  bin: 2.75e1
  variant carriers: 199
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 3.25e1
  variant carriers: 212
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 4.25e1
  variant carriers: 211
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.75e1
  variant carriers: 190
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.75e1
  variant carriers: 217
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 339
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.75e1
  variant carriers: 377
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 2.25e1
  variant carriers: 172
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 235
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.75e1
  variant carriers: 266
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 9.25e1
  variant carriers: 456
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 220
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 5.75e1
  variant carriers: 227
genotype depth: GenotypeDepth
  all individuals: 40195
  bin: 9.75e1
  variant carriers: 39966
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.25e1
  variant carriers: 249
genotype quality: GenotypeQuality
hgvs: p.Leu1833Leu
num of homozygotes: 14542
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/16-15811024-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811024
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811024
    reference: chr 16
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7024A>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7024A>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7024A>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7024A>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5498T>G
  hgvsp: ENSP00000379616.3:p.Leu1833Arg
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5477T>G
  hgvsp: ENSP00000458731.1:p.Leu1826Arg
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3397T>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5498T>G
  hgvsp: ENSP00000407821.2:p.Leu1833Arg
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7024A>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5477T>G
  hgvsp: ENSP00000300036.5:p.Leu1826Arg
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1765T>G
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39063
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1833Arg
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum

16-15811028-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811028
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811028
    reference: chr 16
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5494C>G
  hgvsp: ENSP00000379616.3:p.Gln1832Glu
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1761C>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3393C>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7020G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5473C>G
  hgvsp: ENSP00000300036.5:p.Gln1825Glu
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7020G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5473C>G
  hgvsp: ENSP00000458731.1:p.Gln1825Glu
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7020G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5494C>G
  hgvsp: ENSP00000407821.2:p.Gln1832Glu
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7020G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7020G>C
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39062
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1832Glu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum

16-15811031-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811031
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811031
    reference: chr 16
allele count: 10
allele frequency: 8.241848811525401e-5
allele num: 121332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7017C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5491G>A
  hgvsp: ENSP00000407821.2:p.Ala1831Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7017C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5491G>A
  hgvsp: ENSP00000379616.3:p.Ala1831Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1758G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7017C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5470G>A
  hgvsp: ENSP00000300036.5:p.Ala1824Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5470G>A
  hgvsp: ENSP00000458731.1:p.Ala1824Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3390G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7017C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7017C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39067
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1831Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

16-15811033-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811033
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811033
    reference: chr 16
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5468T>C
  hgvsp: ENSP00000458731.1:p.Ile1823Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5468T>C
  hgvsp: ENSP00000300036.5:p.Ile1823Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7015A>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7015A>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5489T>C
  hgvsp: ENSP00000407821.2:p.Ile1830Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3388T>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7015A>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7015A>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5489T>C
  hgvsp: ENSP00000379616.3:p.Ile1830Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7015A>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1756T>C
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39060
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile1830Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-15811040-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811040
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811040
    reference: chr 16
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7008C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7008C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3381G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5482G>A
  hgvsp: ENSP00000407821.2:p.Ala1828Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5482G>A
  hgvsp: ENSP00000379616.3:p.Ala1828Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7008C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7008C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5461G>A
  hgvsp: ENSP00000458731.1:p.Ala1821Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7008C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5461G>A
  hgvsp: ENSP00000300036.5:p.Ala1821Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1749G>A
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39059
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1828Thr
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

16-15811047-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811047
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811047
    reference: chr 16
allele count: 3
allele frequency: 2.472310126582278e-5
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5454G>A
  hgvsp: ENST00000300036.5:c.5454G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7001C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7001C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3374G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5454G>A
  hgvsp: ENST00000576790.2:c.5454G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5475G>A
  hgvsp: ENST00000396324.3:c.5475G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5475G>A
  hgvsp: ENST00000452625.2:c.5475G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7001C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7001C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7001C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1742G>A
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39059
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1825Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

16-15811048-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811048
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811048
    reference: chr 16
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-7000G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-7000G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-7000G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3373C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1741C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5474C>T
  hgvsp: ENSP00000407821.2:p.Ala1825Val
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5453C>T
  hgvsp: ENSP00000458731.1:p.Ala1818Val
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-7000G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5474C>T
  hgvsp: ENSP00000379616.3:p.Ala1825Val
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-7000G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5453C>T
  hgvsp: ENSP00000300036.5:p.Ala1818Val
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39058
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1825Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

16-15811050-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811050
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811050
    reference: chr 16
allele count: 2
allele frequency: 1.648152421135907e-5
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6998C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6998C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5472G>A
  hgvsp: ENST00000396324.3:c.5472G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5472G>A
  hgvsp: ENST00000452625.2:c.5472G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6998C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1739G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5451G>A
  hgvsp: ENST00000300036.5:c.5451G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3371G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6998C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6998C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5451G>A
  hgvsp: ENST00000576790.2:c.5451G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39058
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1824Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

16-15811051-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811051
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811051
    reference: chr 16
allele count: 11
allele frequency: 9.064838316247487e-5
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3370C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1738C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6997G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5450C>T
  hgvsp: ENSP00000458731.1:p.Ala1817Val
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6997G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5450C>T
  hgvsp: ENSP00000300036.5:p.Ala1817Val
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5471C>T
  hgvsp: ENSP00000379616.3:p.Ala1824Val
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6997G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6997G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6997G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5471C>T
  hgvsp: ENSP00000407821.2:p.Ala1824Val
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39058
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1824Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD

16-15811052-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811052
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811052
    reference: chr 16
allele count: 2
allele frequency: 1.648125257519571e-5
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6996C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6996C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6996C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1737G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5470G>A
  hgvsp: ENSP00000407821.2:p.Ala1824Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6996C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5449G>A
  hgvsp: ENSP00000300036.5:p.Ala1817Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5449G>A
  hgvsp: ENSP00000458731.1:p.Ala1817Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5470G>A
  hgvsp: ENSP00000379616.3:p.Ala1824Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3369G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6996C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39058
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1824Thr
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

16-15811053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811053
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811053
    reference: chr 16
allele count: 3
allele frequency: 2.472269378471478e-5
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5469C>T
  hgvsp: ENST00000396324.3:c.5469C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6995G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6995G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1736C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5469C>T
  hgvsp: ENST00000452625.2:c.5469C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5448C>T
  hgvsp: ENST00000576790.2:c.5448C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3368C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6995G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6995G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6995G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5448C>T
  hgvsp: ENST00000300036.5:c.5448C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39059
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile1823Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

16-15811057-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811057
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811057
    reference: chr 16
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1732C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5465C>T
  hgvsp: ENSP00000379616.3:p.Thr1822Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6991G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5444C>T
  hgvsp: ENSP00000300036.5:p.Thr1815Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6991G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5444C>T
  hgvsp: ENSP00000458731.1:p.Thr1815Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5465C>T
  hgvsp: ENSP00000407821.2:p.Thr1822Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3364C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6991G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6991G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6991G>A
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39057
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1822Ile
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum

16-15811058-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811058
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811058
    reference: chr 16
allele count: 3
allele frequency: 2.472310126582278e-5
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5443A>G
  hgvsp: ENSP00000458731.1:p.Thr1815Ala
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6990T>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6990T>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5464A>G
  hgvsp: ENSP00000379616.3:p.Thr1822Ala
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6990T>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5443A>G
  hgvsp: ENSP00000300036.5:p.Thr1815Ala
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3363A>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5464A>G
  hgvsp: ENSP00000407821.2:p.Thr1822Ala
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6990T>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6990T>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1731A>G
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39057
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1822Ala
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

16-15811060-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811060
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811060
    reference: chr 16
allele count: 22
allele frequency: 1.812997544212417e-4
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6988G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1729C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5462C>T
  hgvsp: ENSP00000379616.3:p.Ser1821Phe
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5441C>T
  hgvsp: ENSP00000300036.5:p.Ser1814Phe
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5462C>T
  hgvsp: ENSP00000407821.2:p.Ser1821Phe
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6988G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6988G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5441C>T
  hgvsp: ENSP00000458731.1:p.Ser1814Phe
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6988G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3361C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6988G>A
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39058
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
hgvs: p.Ser1821Phe
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

16-15811062-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811062
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811062
    reference: chr 16
allele count: 58517
allele frequency: 4.822962169290365e-1
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6986C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5439G>A
  hgvsp: ENST00000300036.5:c.5439G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5460G>A
  hgvsp: ENST00000452625.2:c.5460G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6986C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5439G>A
  hgvsp: ENST00000576790.2:c.5439G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5460G>A
  hgvsp: ENST00000396324.3:c.5460G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6986C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3359G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6986C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6986C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1727G>A
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.25e1
  variant carriers: 480
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 369
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 6425
  bin: 2.75e1
  variant carriers: 182
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 4.25e1
  variant carriers: 215
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 3.75e1
  variant carriers: 237
genotype depth: GenotypeDepth
  all individuals: 39763
  bin: 9.75e1
  variant carriers: 39575
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 2.25e1
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.25e1
  variant carriers: 408
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 308
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 3.25e1
  variant carriers: 234
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.75e1
  variant carriers: 267
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 4.75e1
  variant carriers: 251
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 8.75e1
  variant carriers: 482
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 5.25e1
  variant carriers: 228
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 5.75e1
  variant carriers: 250
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 238
genotype quality: GenotypeQuality
hgvs: p.Lys1820Lys
num of homozygotes: 14576
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

16-15811071-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811071
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811071
    reference: chr 16
allele count: 4
allele frequency: 3.297391763115376e-5
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6977G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6977G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5451C>T
  hgvsp: ENST00000452625.2:c.5451C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5451C>T
  hgvsp: ENST00000396324.3:c.5451C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6977G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3350C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5430C>T
  hgvsp: ENST00000576790.2:c.5430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5430C>T
  hgvsp: ENST00000300036.5:c.5430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1718C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6977G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6977G>A
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17454
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1817Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-15811073-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811073
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811073
    reference: chr 16
allele count: 4
allele frequency: 3.297500494625074e-5
allele num: 121304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1716T>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5428T>C
  hgvsp: ENSP00000458731.1:p.Ser1810Pro
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6975A>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5449T>C
  hgvsp: ENSP00000379616.3:p.Ser1817Pro
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6975A>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5449T>C
  hgvsp: ENSP00000407821.2:p.Ser1817Pro
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6975A>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6975A>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3348T>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5428T>C
  hgvsp: ENSP00000300036.5:p.Ser1810Pro
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6975A>G
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1817Pro
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP

16-15811077-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811077
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811077
    reference: chr 16
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6971G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6971G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3344C>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5424C>G
  hgvsp: ENST00000300036.5:c.5424C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5445C>G
  hgvsp: ENST00000452625.2:c.5445C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6971G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6971G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5424C>G
  hgvsp: ENST00000576790.2:c.5424C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1712C>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5445C>G
  hgvsp: ENST00000396324.3:c.5445C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6971G>C
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val1815Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

16-15811079-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811079
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811079
    reference: chr 16
allele count: 4
allele frequency: 3.297881111385935e-5
allele num: 121290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5422G>A
  hgvsp: ENSP00000300036.5:p.Val1808Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5443G>A
  hgvsp: ENSP00000379616.3:p.Val1815Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5422G>A
  hgvsp: ENSP00000458731.1:p.Val1808Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1710G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5443G>A
  hgvsp: ENSP00000407821.2:p.Val1815Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6969C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6969C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3342G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6969C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6969C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6969C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val1815Ile
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-15811080-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811080
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811080
    reference: chr 16
allele count: 5
allele frequency: 4.122351389232418e-5
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5442C>T
  hgvsp: ENST00000396324.3:c.5442C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6968G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5421C>T
  hgvsp: ENST00000576790.2:c.5421C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6968G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1709C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5421C>T
  hgvsp: ENST00000300036.5:c.5421C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5442C>T
  hgvsp: ENST00000452625.2:c.5442C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6968G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6968G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6968G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3341C>T
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Ala1814Ala
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: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

16-15811080-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811080
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811080
    reference: chr 16
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5421C>A
  hgvsp: ENST00000300036.5:c.5421C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5442C>A
  hgvsp: ENST00000396324.3:c.5442C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6968G>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1709C>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5442C>A
  hgvsp: ENST00000452625.2:c.5442C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5421C>A
  hgvsp: ENST00000576790.2:c.5421C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6968G>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6968G>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6968G>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3341C>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6968G>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1814Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-15811081-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811081
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811081
    reference: chr 16
allele count: 2
allele frequency: 1.648913366091746e-5
allele num: 121292
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3340C>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6967G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5441C>G
  hgvsp: ENSP00000379616.3:p.Ala1814Gly
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5441C>G
  hgvsp: ENSP00000407821.2:p.Ala1814Gly
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6967G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1708C>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5420C>G
  hgvsp: ENSP00000300036.5:p.Ala1807Gly
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6967G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5420C>G
  hgvsp: ENSP00000458731.1:p.Ala1807Gly
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6967G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6967G>C
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1814Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

16-15811089-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811089
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811089
    reference: chr 16
allele count: 3
allele frequency: 2.473655568198684e-5
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5433G>A
  hgvsp: ENSP00000379616.3:p.Met1811Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6959C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6959C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6959C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5433G>A
  hgvsp: ENSP00000407821.2:p.Met1811Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3332G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6959C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5412G>A
  hgvsp: ENSP00000300036.5:p.Met1804Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6959C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5412G>A
  hgvsp: ENSP00000458731.1:p.Met1804Ile
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1700G>A
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1811Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

16-15811091-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811091
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811091
    reference: chr 16
allele count: 2
allele frequency: 1.649185302460584e-5
allele num: 121272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6957T>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5431A>C
  hgvsp: ENSP00000379616.3:p.Met1811Leu
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6957T>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3330A>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5410A>C
  hgvsp: ENSP00000458731.1:p.Met1804Leu
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6957T>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5431A>C
  hgvsp: ENSP00000407821.2:p.Met1811Leu
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5410A>C
  hgvsp: ENSP00000300036.5:p.Met1804Leu
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6957T>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1698A>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6957T>G
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22916
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1811Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

16-15811092-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811092
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811092
    reference: chr 16
allele count: 2
allele frequency: 1.64923970049807e-5
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5430G>A
  hgvsp: ENST00000396324.3:c.5430G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5409G>A
  hgvsp: ENST00000576790.2:c.5409G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1697G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6956C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6956C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6956C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3329G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6956C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5409G>A
  hgvsp: ENST00000300036.5:c.5409G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5430G>A
  hgvsp: ENST00000452625.2:c.5430G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6956C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu1810Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

16-15811095-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811095
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811095
    reference: chr 16
allele count: 4
allele frequency: 3.298588204248581e-5
allele num: 121264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6953G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6953G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5406C>T
  hgvsp: ENST00000300036.5:c.5406C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6953G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5427C>T
  hgvsp: ENST00000452625.2:c.5427C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5427C>T
  hgvsp: ENST00000396324.3:c.5427C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6953G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3326C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6953G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5406C>T
  hgvsp: ENST00000576790.2:c.5406C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1694C>T
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His1809His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-15811095-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811095
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811095
    reference: chr 16
allele count: 5
allele frequency: 4.123235255310727e-5
allele num: 121264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5427C>G
  hgvsp: ENSP00000407821.2:p.His1809Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5406C>G
  hgvsp: ENSP00000300036.5:p.His1802Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1694C>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5406C>G
  hgvsp: ENSP00000458731.1:p.His1802Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6953G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3326C>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6953G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6953G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5427C>G
  hgvsp: ENSP00000379616.3:p.His1809Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6953G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6953G>C
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 22903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His1809Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-15811105-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811105
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811105
    reference: chr 16
allele count: 2
allele frequency: 1.649457328538911e-5
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5417G>A
  hgvsp: ENSP00000407821.2:p.Ser1806Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6943C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5396G>A
  hgvsp: ENSP00000300036.5:p.Ser1799Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1684G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5396G>A
  hgvsp: ENSP00000458731.1:p.Ser1799Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6943C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3316G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5417G>A
  hgvsp: ENSP00000379616.3:p.Ser1806Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6943C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6943C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6943C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1806Asn
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

16-15811108-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811108
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811108
    reference: chr 16
allele count: 13
allele frequency: 1.072288759114455e-4
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6940C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3313G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5393G>A
  hgvsp: ENSP00000300036.5:p.Arg1798Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5393G>A
  hgvsp: ENSP00000458731.1:p.Arg1798Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5414G>A
  hgvsp: ENSP00000407821.2:p.Arg1805Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1681G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6940C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6940C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6940C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5414G>A
  hgvsp: ENSP00000379616.3:p.Arg1805Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6940C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1805Gln
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: C
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff

16-15811109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811109
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811109
    reference: chr 16
allele count: 2
allele frequency: 1.649783878311941e-5
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3312C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1680C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5392C>T
  hgvsp: ENSP00000458731.1:p.Arg1798Trp
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5413C>T
  hgvsp: ENSP00000407821.2:p.Arg1805Trp
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5413C>T
  hgvsp: ENSP00000379616.3:p.Arg1805Trp
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6939G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6939G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6939G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5392C>T
  hgvsp: ENSP00000300036.5:p.Arg1798Trp
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6939G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6939G>A
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1805Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

16-15811116-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811116
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811116
    reference: chr 16
allele count: 2
allele frequency: 1.650273945474949e-5
allele num: 121192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5406G>C
  hgvsp: ENSP00000407821.2:p.Lys1802Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6932C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5406G>C
  hgvsp: ENSP00000379616.3:p.Lys1802Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6932C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5385G>C
  hgvsp: ENSP00000458731.1:p.Lys1795Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5385G>C
  hgvsp: ENSP00000300036.5:p.Lys1795Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6932C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6932C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6932C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1673G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3305G>C
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys1802Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

16-15811122-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811122
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811122
    reference: chr 16
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: G
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5379G>C
  hgvsp: ENSP00000300036.5:p.Gln1793His
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3299G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5400G>C
  hgvsp: ENSP00000407821.2:p.Gln1800His
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6926C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6926C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5400G>C
  hgvsp: ENSP00000379616.3:p.Gln1800His
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1667G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5379G>C
  hgvsp: ENSP00000458731.1:p.Gln1793His
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6926C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6926C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6926C>G
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1800His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD

16-15811122-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811122
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811122
    reference: chr 16
allele count: 3
allele frequency: 2.476269087907552e-5
allele num: 121150
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5400G>A
  hgvsp: ENST00000452625.2:c.5400G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6926C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6926C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6926C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5379G>A
  hgvsp: ENST00000576790.2:c.5379G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3299G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5400G>A
  hgvsp: ENST00000396324.3:c.5400G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5379G>A
  hgvsp: ENST00000300036.5:c.5379G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6926C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1667G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6926C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17348
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1800Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD

16-15811126-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811126
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811126
    reference: chr 16
allele count: 2
allele frequency: 1.651145895251304e-5
allele num: 121128
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3295G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5375G>A
  hgvsp: ENSP00000300036.5:p.Arg1792Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5375G>A
  hgvsp: ENSP00000458731.1:p.Arg1792Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5396G>A
  hgvsp: ENSP00000379616.3:p.Arg1799Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1663G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6922C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6922C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6922C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6922C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5396G>A
  hgvsp: ENSP00000407821.2:p.Arg1799Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6922C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1799Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

16-15811130-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811130
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811130
    reference: chr 16
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1659G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6918C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6918C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6918C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5371G>C
  hgvsp: ENSP00000458731.1:p.Glu1791Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3291G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5371G>C
  hgvsp: ENSP00000300036.5:p.Glu1791Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6918C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6918C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5392G>C
  hgvsp: ENSP00000407821.2:p.Glu1798Gln
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5392G>C
  hgvsp: ENSP00000379616.3:p.Glu1798Gln
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu1798Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

16-15811130-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811130
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811130
    reference: chr 16
allele count: 2
allele frequency: 1.65144584083365e-5
allele num: 121106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1659G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5371G>A
  hgvsp: ENSP00000300036.5:p.Glu1791Lys
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6918C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6918C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5371G>A
  hgvsp: ENSP00000458731.1:p.Glu1791Lys
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3291G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5392G>A
  hgvsp: ENSP00000379616.3:p.Glu1798Lys
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5392G>A
  hgvsp: ENSP00000407821.2:p.Glu1798Lys
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6918C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6918C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6918C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu1798Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

16-15811131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811131
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811131
    reference: chr 16
allele count: 2068
allele frequency: 1.707764216228715e-2
allele num: 121094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1658C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6917G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6917G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5391C>T
  hgvsp: ENST00000452625.2:c.5391C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3290C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6917G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5391C>T
  hgvsp: ENST00000396324.3:c.5391C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6917G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5370C>T
  hgvsp: ENST00000300036.5:c.5370C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5370C>T
  hgvsp: ENST00000576790.2:c.5370C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6917G>A
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 6155
  bin: 3.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 22819
  bin: 2.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4373
  bin: 2.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 17300
  bin: 3.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 4.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 9.75e1
  variant carriers: 1332
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 4.75e1
  variant carriers: 32
genotype quality: GenotypeQuality
hgvs: p.Leu1797Leu
num of homozygotes: 105
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

16-15811131-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811131
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811131
    reference: chr 16
allele count: 1
allele frequency: 8.258047467256841e-6
allele num: 121094
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6917G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1658C>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6917G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5391C>G
  hgvsp: ENST00000396324.3:c.5391C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5391C>G
  hgvsp: ENST00000452625.2:c.5391C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5370C>G
  hgvsp: ENST00000576790.2:c.5370C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6917G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6917G>C
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3290C>G
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5370C>G
  hgvsp: ENST00000300036.5:c.5370C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6917G>C
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1797Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

16-15811133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811133
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811133
    reference: chr 16
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3288C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6915G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5368C>T
  hgvsp: ENSP00000300036.5:p.Leu1790Phe
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5389C>T
  hgvsp: ENSP00000379616.3:p.Leu1797Phe
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5389C>T
  hgvsp: ENSP00000407821.2:p.Leu1797Phe
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6915G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6915G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5368C>T
  hgvsp: ENSP00000458731.1:p.Leu1790Phe
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1656C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6915G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6915G>A
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1797Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ

16-15811134-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811134
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811134
    reference: chr 16
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5367G>A
  hgvsp: ENST00000300036.5:c.5367G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5388G>A
  hgvsp: ENST00000452625.2:c.5388G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1655G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5388G>A
  hgvsp: ENST00000396324.3:c.5388G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6914C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6914C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3287G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5367G>A
  hgvsp: ENST00000576790.2:c.5367G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6914C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6914C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6914C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1796Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

16-15811142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811142
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811142
    reference: chr 16
allele count: 1
allele frequency: 8.265829062654984e-6
allele num: 120980
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5380C>T
  hgvsp: ENSP00000379616.3:p.Arg1794Trp
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6906G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5359C>T
  hgvsp: ENSP00000300036.5:p.Arg1787Trp
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1647C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5359C>T
  hgvsp: ENSP00000458731.1:p.Arg1787Trp
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3279C>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6906G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6906G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5380C>T
  hgvsp: ENSP00000407821.2:p.Arg1794Trp
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6906G>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6906G>A
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg1794Trp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

16-15811145-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811145
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811145
    reference: chr 16
allele count: 1
allele frequency: 8.267195767195768e-6
allele num: 120960
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6903C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5377G>A
  hgvsp: ENSP00000379616.3:p.Ala1793Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5356G>A
  hgvsp: ENSP00000458731.1:p.Ala1786Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5377G>A
  hgvsp: ENSP00000407821.2:p.Ala1793Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6903C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6903C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3276G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5356G>A
  hgvsp: ENSP00000300036.5:p.Ala1786Thr
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1644G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6903C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6903C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1793Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

16-15811147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811147
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811147
    reference: chr 16
allele count: 1
allele frequency: 8.269109913008963e-6
allele num: 120932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1642G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6901C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5375G>A
  hgvsp: ENSP00000407821.2:p.Ser1792Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3274G>A
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5375G>A
  hgvsp: ENSP00000379616.3:p.Ser1792Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6901C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6901C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5354G>A
  hgvsp: ENSP00000300036.5:p.Ser1785Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5354G>A
  hgvsp: ENSP00000458731.1:p.Ser1785Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6901C>T
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6901C>T
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23501
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1792Asn
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ

16-15811148-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811148
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811148
    reference: chr 16
allele count: 16
allele frequency: 1.323407775020678e-4
allele num: 120900
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6900T>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5374A>T
  hgvsp: ENSP00000407821.2:p.Ser1792Cys
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5353A>T
  hgvsp: ENSP00000458731.1:p.Ser1785Cys
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1641A>T
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5353A>T
  hgvsp: ENSP00000300036.5:p.Ser1785Cys
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6900T>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6900T>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5374A>T
  hgvsp: ENSP00000379616.3:p.Ser1792Cys
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6900T>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6900T>A
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3273A>T
  variant of: http://identifiers.org/hgnc/7569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
hgvs: p.Ser1792Cys
num of homozygotes: 1
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

16-15811155-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15811155
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15811155
    reference: chr 16
allele count: 1
allele frequency: 8.276364358664525e-6
allele num: 120826
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000345892
  ensembl transcript: ENST00000342673
  gene symbol: NDE1
  hgvsc: ENST00000342673.5:c.948-6893C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000300036
  ensembl transcript: ENST00000300036
  gene symbol: MYH11
  hgvsc: ENST00000300036.5:c.5346G>C
  hgvsp: ENSP00000300036.5:p.Lys1782Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000576164
  gene symbol: MYH11
  hgvsc: ENST00000576164.1:n.3266G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459918
  ensembl transcript: ENST00000572967
  gene symbol: NDE1
  hgvsc: ENST00000572967.1:c.*33-6893C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133392
  ensembl transcript: ENST00000571275
  gene symbol: MYH11
  hgvsc: ENST00000571275.1:n.1634G>C
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000459863
  ensembl transcript: ENST00000573694
  gene symbol: NDE1
  hgvsc: ENST00000573694.1:c.380-6893C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000458731
  ensembl transcript: ENST00000576790
  gene symbol: MYH11
  hgvsc: ENST00000576790.2:c.5346G>C
  hgvsp: ENSP00000458731.1:p.Lys1782Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379642
  ensembl transcript: ENST00000396354
  gene symbol: NDE1
  hgvsc: ENST00000396354.1:c.948-6893C>G
  variant of: http://identifiers.org/hgnc/17619
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000379616
  ensembl transcript: ENST00000396324
  gene symbol: MYH11
  hgvsc: ENST00000396324.3:c.5367G>C
  hgvsp: ENSP00000379616.3:p.Lys1789Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133392
  ensembl protein: ENSP00000407821
  ensembl transcript: ENST00000452625
  gene symbol: MYH11
  hgvsc: ENST00000452625.2:c.5367G>C
  hgvsp: ENSP00000407821.2:p.Lys1789Asn
  variant of: http://identifiers.org/hgnc/7569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072864
  ensembl protein: ENSP00000379643
  ensembl transcript: ENST00000396355
  gene symbol: NDE1
  hgvsc: ENST00000396355.1:c.948-6893C>G
  variant of: http://identifiers.org/hgnc/17619
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys1789Asn
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 8107
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43803
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 968
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 133
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1444
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3271
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 466
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 644
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.350499684883407e-4
allele num: 66642
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

QD
type: SiteQuality
SIO_000300: 1.211e1

FS
type: SiteQuality
SIO_000300: 2.471e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.968e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

DP
type: SiteQuality
SIO_000300: 4.890651e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-1

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

GenotypeQuality
all individuals: 131
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8128
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43802
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 967
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 145
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3272
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
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: 16500
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 7
allele frequency: 8.098102730217492e-4
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.21e-1

QD
type: SiteQuality
SIO_000300: 1.261e1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.638e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-2

DP
type: SiteQuality
SIO_000300: 4.89092e6

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

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

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8128
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 43802
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 967
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 6.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.638e0

QD
type: SiteQuality
SIO_000300: 1.261e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.89092e6

MQ
type: SiteQuality
SIO_000300: 5.961e1

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

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

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

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8158
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3276
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43804
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.25e-1

FS
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

VQSLOD
type: SiteQuality
SIO_000300: -5.91e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.24e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.995e0

QD
type: SiteQuality
SIO_000300: 8.720000000000001e0

DP
type: SiteQuality
SIO_000300: 4.891144e6

GenotypeQuality
all individuals: 1199
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8190
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3284
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
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: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

MQ
type: SiteQuality
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QD
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MQRankSum
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SIO_000300: 1.03e0

InbreedingCoeff
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SIO_000300: -1.0e-4

DP
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SIO_000300: 4.891601e6

FS
type: SiteQuality
SIO_000300: 7.061e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.702e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
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SIO_000300: 1.79e0

ReadPosRankSum
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MQ
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FS
type: SiteQuality
SIO_000300: 1.341e0

DP
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SIO_000300: 4.891988e6

MQRankSum
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SIO_000300: 1.47e-1

BaseQRankSum
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SIO_000300: -1.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.46e-1

QD
type: SiteQuality
SIO_000300: 1.385e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.207505518763797e-3
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.269e0

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.928e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.74e-1

MQRankSum
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SIO_000300: -5.570000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.126e0

DP
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SIO_000300: 4.892505e6

QD
type: SiteQuality
SIO_000300: 1.237e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.22e0

QD
type: SiteQuality
SIO_000300: 1.185e1

VQSLOD
type: SiteQuality
SIO_000300: 3.48e0

DP
type: SiteQuality
SIO_000300: 4.892922e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 1.977e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

GenotypeQuality
all individuals: 644
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
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: 11564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.977e0

VQSLOD
type: SiteQuality
SIO_000300: 3.48e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
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SIO_000300: 1.0e-4

ReadPosRankSum
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SIO_000300: 2.24e-1

DP
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SIO_000300: 4.892922e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.22e0

QD
type: SiteQuality
SIO_000300: 1.185e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 201

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000660145231951e-5
allele num: 66652
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.649022660439371e-4
allele num: 11562
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 188
allele frequency: 1.815723391925826e-2
allele num: 10354
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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FS
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QD
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DP
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MQRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.964e1

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.20026405809278e-4
allele num: 66652
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.818181818181818e-4
allele num: 16500
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.154e1

InbreedingCoeff
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MQRankSum
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MQ
type: SiteQuality
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VQSLOD
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DP
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ReadPosRankSum
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FS
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ClippingRankSum
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SIO_000300: -2.39e-1

BaseQRankSum
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
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: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.197e0

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

European (Non-Finnish)
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allele num: 66658
num of homozygotes: 0

Latino
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Other
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South Asian
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East Asian
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European (Finnish)
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele num: 66658
num of homozygotes: 0

East Asian
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Other
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South Asian
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African
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European (Finnish)
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Latino
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DP
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FS
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQ
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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European (Finnish)
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Other
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East Asian
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South Asian
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DP
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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South Asian
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QD
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FS
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3358
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43693
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -3.207e-1

DP
type: SiteQuality
SIO_000300: 4.89536e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.55e-1

QD
type: SiteQuality
SIO_000300: 8.220000000000001e0

FS
type: SiteQuality
SIO_000300: 5.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 652
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 102
bin: 2.25e1
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GenotypeQuality
all individuals: 8496
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
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GenotypeQuality
all individuals: 3360
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 996
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 477
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1212
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43693
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000390050706592e-5
allele num: 66658
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: -2.49e-1

QD
type: SiteQuality
SIO_000300: 1.08e1

MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 2.488e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.187e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.09e-1

DP
type: SiteQuality
SIO_000300: 4.895789e6

VQSLOD
type: SiteQuality
SIO_000300: 9.370000000000001e-1

GenotypeQuality
all individuals: 1216
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8493
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variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 3363
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variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

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

GenotypeQuality
all individuals: 652
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1471
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

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

GenotypeQuality
all individuals: 43693
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 477
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.453e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.85e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 9.35e0

DP
type: SiteQuality
SIO_000300: 4.895814e6

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 14

GenotypeQuality
all individuals: 371
bin: 8.75e1
variant carriers: 18

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 4

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 11

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 9

GenotypeQuality
all individuals: 7805
bin: 6.25e1
variant carriers: 23

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1044
bin: 7.25e1
variant carriers: 20

GenotypeQuality
all individuals: 503
bin: 9.25e1
variant carriers: 28

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 6

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

GenotypeQuality
all individuals: 3076
bin: 6.75e1
variant carriers: 21

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 11

GenotypeQuality
all individuals: 856
bin: 8.25e1
variant carriers: 32

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1275
bin: 7.75e1
variant carriers: 27

GenotypeQuality
all individuals: 45564
bin: 9.75e1
variant carriers: 43667

Other
type: Population
allele count: 447
allele frequency: 4.933774834437086e-1
allele num: 906
num of homozygotes: 114

Latino
type: Population
allele count: 6667
allele frequency: 5.767301038062284e-1
allele num: 11560
num of homozygotes: 1962

African
type: Population
allele count: 3080
allele frequency: 2.968388589051658e-1
allele num: 10376
num of homozygotes: 470

European (Finnish)
type: Population
allele count: 3461
allele frequency: 5.23283943150892e-1
allele num: 6614
num of homozygotes: 908

East Asian
type: Population
allele count: 2682
allele frequency: 3.103448275862069e-1
allele num: 8642
num of homozygotes: 442

South Asian
type: Population
allele count: 7872
allele frequency: 4.768597043857524e-1
allele num: 16508
num of homozygotes: 1913

European (Non-Finnish)
type: Population
allele count: 34229
allele frequency: 5.132707533589251e-1
allele num: 66688
num of homozygotes: 8733

DP
type: SiteQuality
SIO_000300: 8.367497e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

FS
type: SiteQuality
SIO_000300: 5.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.99e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.019e0

QD
type: SiteQuality
SIO_000300: 1.84e1

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

GenotypeQuality
all individuals: 1114
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 585
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1369
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52
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variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8063
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44676
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 425
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3196
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

QD
type: SiteQuality
SIO_000300: 1.326e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.444e0

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

DP
type: SiteQuality
SIO_000300: 7.597202e6

FS
type: SiteQuality
SIO_000300: 4.186e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

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

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 44674
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variant carriers: 2

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 1115
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variant carriers: 0

GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 1369
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variant carriers: 0

GenotypeQuality
all individuals: 3187
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variant carriers: 0

GenotypeQuality
all individuals: 425
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variant carriers: 0

GenotypeQuality
all individuals: 8074
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variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.88e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.205e1

FS
type: SiteQuality
SIO_000300: 3.95e-1

DP
type: SiteQuality
SIO_000300: 7.597045e6

MQRankSum
type: SiteQuality
SIO_000300: 5.04e-1

GenotypeQuality
all individuals: 425
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44676
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 3194
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variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 1113
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variant carriers: 0

GenotypeQuality
all individuals: 54
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GenotypeQuality
all individuals: 584
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GenotypeQuality
all individuals: 970
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

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

GenotypeQuality
all individuals: 1368
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variant carriers: 0

GenotypeQuality
all individuals: 8081
bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 9.624639076034649e-4
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.97e0

QD
type: SiteQuality
SIO_000300: 1.215e1

DP
type: SiteQuality
SIO_000300: 7.597618e6

MQRankSum
type: SiteQuality
SIO_000300: 3.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.16e-1

FS
type: SiteQuality
SIO_000300: 5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.747e0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
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GenotypeQuality
all individuals: 584
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 424
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 3197
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GenotypeQuality
all individuals: 971
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variant carriers: 0

GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 1113
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GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 1369
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GenotypeQuality
all individuals: 44668
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8104
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.992e1

ClippingRankSum
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BaseQRankSum
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QD
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VQSLOD
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DP
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FS
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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European (Finnish)
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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East Asian
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Other
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Latino
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African
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European (Finnish)
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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Latino
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South Asian
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African
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East Asian
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Other
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FS
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MQ
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ClippingRankSum
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DP
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VQSLOD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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East Asian
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African
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South Asian
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Latino
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Other
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MQRankSum
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QD
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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African
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Other
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European (Non-Finnish)
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South Asian
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East Asian
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ReadPosRankSum
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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QD
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DP
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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African
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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BaseQRankSum
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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African
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European (Non-Finnish)
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South Asian
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ReadPosRankSum
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VQSLOD
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DP
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MQRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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MQ
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3200
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.988e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.212e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

DP
type: SiteQuality
SIO_000300: 7.596813e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.333e0

QD
type: SiteQuality
SIO_000300: 1.115e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e0

GenotypeQuality
all individuals: 423
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44665
bin: 9.75e1
variant carriers: 3

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.763e0

QD
type: SiteQuality
SIO_000300: 1.381e1

MQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

DP
type: SiteQuality
SIO_000300: 7.597019e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.009e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

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

GenotypeQuality
all individuals: 1107
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variant carriers: 0

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 22

GenotypeQuality
all individuals: 423
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 980
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GenotypeQuality
all individuals: 583
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 20
allele frequency: 2.998410842253605e-4
allele num: 66702
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.359e1

MQRankSum
type: SiteQuality
SIO_000300: 2.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.484e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 3.215e0

DP
type: SiteQuality
SIO_000300: 7.597622e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.73e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
all individuals: 45551
bin: 9.75e1
variant carriers: 43724

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 6

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 7

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 7

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 7864
bin: 6.25e1
variant carriers: 17

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 8

GenotypeQuality
all individuals: 370
bin: 8.75e1
variant carriers: 18

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 12

GenotypeQuality
all individuals: 1274
bin: 7.75e1
variant carriers: 24

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 4

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

GenotypeQuality
all individuals: 3084
bin: 6.75e1
variant carriers: 21

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 7

GenotypeQuality
all individuals: 512
bin: 9.25e1
variant carriers: 38

GenotypeQuality
all individuals: 1043
bin: 7.25e1
variant carriers: 19

GenotypeQuality
all individuals: 854
bin: 8.25e1
variant carriers: 28

European (Non-Finnish)
type: Population
allele count: 34312
allele frequency: 5.143302554263101e-1
allele num: 66712
num of homozygotes: 8766

Latino
type: Population
allele count: 6670
allele frequency: 5.766902991526889e-1
allele num: 11566
num of homozygotes: 1963

East Asian
type: Population
allele count: 2682
allele frequency: 3.105604446503011e-1
allele num: 8636
num of homozygotes: 442

South Asian
type: Population
allele count: 7874
allele frequency: 4.769808577659317e-1
allele num: 16508
num of homozygotes: 1913

African
type: Population
allele count: 3069
allele frequency: 2.953801732435034e-1
allele num: 10390
num of homozygotes: 469

European (Finnish)
type: Population
allele count: 3463
allele frequency: 5.237447065940714e-1
allele num: 6612
num of homozygotes: 909

Other
type: Population
allele count: 447
allele frequency: 4.933774834437086e-1
allele num: 906
num of homozygotes: 114

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.01e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 1.104e0

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.11e-1

DP
type: SiteQuality
SIO_000300: 7.930851e6

QD
type: SiteQuality
SIO_000300: 1.906e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.2e0

GenotypeQuality
all individuals: 28459
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 3513
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variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 4320
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 7491
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variant carriers: 4

GenotypeQuality
all individuals: 11198
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 1610
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variant carriers: 0

GenotypeQuality
all individuals: 2755
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817520901490367e-4
allele num: 16506
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.609e0

MQRankSum
type: SiteQuality
SIO_000300: -8.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

QD
type: SiteQuality
SIO_000300: 1.221e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.484e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

DP
type: SiteQuality
SIO_000300: 2.154983e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 1610
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 28470
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 29
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7487
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variant carriers: 4

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 2757
bin: 8.25e1
variant carriers: 0

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

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

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999490086685263e-5
allele num: 66678
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

QD
type: SiteQuality
SIO_000300: 1.25e1

DP
type: SiteQuality
SIO_000300: 2.154434e6

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

GenotypeQuality
all individuals: 11203
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 7482
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 11
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GenotypeQuality
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 4316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
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: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.168e-1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.18e-1

DP
type: SiteQuality
SIO_000300: 2.153962e6

FS
type: SiteQuality
SIO_000300: 4.322e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.093e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.090000000000001e-1

GenotypeQuality
all individuals: 2756
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 86
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GenotypeQuality
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 7481
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variant carriers: 4

GenotypeQuality
all individuals: 11195
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.313743637204998e-4
allele num: 8644
num of homozygotes: 0

African
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allele count: 0
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South Asian
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European (Finnish)
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MQ
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QD
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VQSLOD
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FS
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BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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South Asian
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ClippingRankSum
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MQ
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DP
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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FS
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MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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ClippingRankSum
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QD
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MQ
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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Latino
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African
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Other
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East Asian
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ClippingRankSum
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QD
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MQ
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BaseQRankSum
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FS
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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MQRankSum
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BaseQRankSum
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MQ
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QD
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DP
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InbreedingCoeff
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FS
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Other
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East Asian
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European (Finnish)
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Latino
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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QD
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MQRankSum
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ReadPosRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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South Asian
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Latino
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African
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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FS
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MQRankSum
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MQ
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QD
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DP
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East Asian
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European (Non-Finnish)
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South Asian
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African
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Latino
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European (Finnish)
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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QD
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FS
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SIO_000300: 5.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

GenotypeQuality
all individuals: 4313
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2751
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.502325720973501e-5
allele num: 66646
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

BaseQRankSum
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SIO_000300: 2.02e0

MQ
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SIO_000300: 5.955e1

QD
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FS
type: SiteQuality
SIO_000300: 5.31e-1

DP
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MQRankSum
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SIO_000300: -3.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.001380635092142e-5
allele num: 66636
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.09e-1

ReadPosRankSum
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DP
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SIO_000300: 2.148239e6

QD
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BaseQRankSum
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FS
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SIO_000300: 7.217e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

VQSLOD
type: SiteQuality
SIO_000300: 4.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 13

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

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

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

African
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allele count: 11
allele frequency: 1.060138781804163e-3
allele num: 10376
num of homozygotes: 0

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

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

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

South Asian
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allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

VQSLOD
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SIO_000300: 3.13e0

MQ
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SIO_000300: 5.948e1

QD
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SIO_000300: 1.559e1

BaseQRankSum
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MQRankSum
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SIO_000300: 2.66e-1

ReadPosRankSum
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SIO_000300: 3.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

DP
type: SiteQuality
SIO_000300: 2.14798e6

FS
type: SiteQuality
SIO_000300: 5.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.04e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

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

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

East Asian
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allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

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

African
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allele count: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 5.21e-1

BaseQRankSum
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 4.0e-4

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

QD
type: SiteQuality
SIO_000300: 1.344e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003093185981561e-5
allele num: 66598
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.502133028901039e-5
allele num: 66572
num of homozygotes: 0

African
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East Asian
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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DP
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FS
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QD
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SIO_000300: 1.257e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.658103148541626e-5
allele num: 10354
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.004266057802079e-5
allele num: 66572
num of homozygotes: 0

Latino
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Other
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VQSLOD
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DP
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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ClippingRankSum
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MQ
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QD
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SIO_000300: 1.257e1

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

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.00507858280494e-5
allele num: 66554
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

African
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allele frequency: 9.663703131039814e-5
allele num: 10348
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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MQRankSum
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QD
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ClippingRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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VQSLOD
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MQ
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SIO_000300: 5.972e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.005710850616171e-5
allele num: 66540
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

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

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

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

MQ
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SIO_000300: 5.972e1

FS
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ClippingRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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SIO_000300: 1.18e0

GenotypeQuality
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variant carriers: 1

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

Other
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allele count: 7
allele frequency: 7.72626931567329e-3
allele num: 906
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
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allele count: 32
allele frequency: 4.809715625563639e-4
allele num: 66532
num of homozygotes: 0

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

African
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allele count: 1077
allele frequency: 1.040982022037502e-1
allele num: 10346
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South Asian
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allele count: 895
allele frequency: 5.422270689446262e-2
allele num: 16506
num of homozygotes: 43

Latino
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allele count: 56
allele frequency: 4.840940525587829e-3
allele num: 11568
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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MQ
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DP
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.83e-1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503036132988637e-5
allele num: 66532
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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FS
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VQSLOD
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BaseQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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African
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allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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InbreedingCoeff
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QD
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VQSLOD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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DP
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FS
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MQ
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66528
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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Other
type: Population
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Latino
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allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

European (Finnish)
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South Asian
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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DP
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.85e0

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

DP
type: SiteQuality
SIO_000300: 1.975334e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.28e-1

QD
type: SiteQuality
SIO_000300: 1.13e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.21e-1

FS
type: SiteQuality
SIO_000300: 4.619e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3568
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4405
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11424
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29213
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5756
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66460
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.251e1

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 2.0031e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.973924e6

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11416
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3563
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.377e0

VQSLOD
type: SiteQuality
SIO_000300: 2.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.335e0

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 1.973467e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.214e0

QD
type: SiteQuality
SIO_000300: 1.004e1

MQ
type: SiteQuality
SIO_000300: 5.955e1

GenotypeQuality
all individuals: 3562
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5753
bin: 9.75e1
variant carriers: 15

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

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

GenotypeQuality
all individuals: 100
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11398
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4401
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29115
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2790
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.818843215714805e-4
allele num: 16494
num of homozygotes: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

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

Latino
type: Population
allele count: 11
allele frequency: 9.513924926483308e-4
allele num: 11562
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.972372e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.209e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.72e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.83e-1

QD
type: SiteQuality
SIO_000300: 1.359e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

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

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

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

GenotypeQuality
all individuals: 1628
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0