3-123471128-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471128
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471128
    reference: chr 3
allele count: 1
allele frequency: 8.274036074797286e-6
allele num: 120860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.373+50C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.373+50C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.373+50C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.373+50C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.373+50C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.419+50C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12280C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.732+50C>T
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38517
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

3-123471128-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471128
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471128
    reference: chr 3
allele count: 1
allele frequency: 8.274036074797286e-6
allele num: 120860
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.373+50C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.373+50C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.732+50C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.373+50C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.373+50C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.373+50C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12280C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.419+50C>G
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29983
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38517
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-123471133-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471133
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471133
    reference: chr 3
allele count: 1
allele frequency: 8.272256506129742e-6
allele num: 120886
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.373+45G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.419+45G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.373+45G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.373+45G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.373+45G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.373+45G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12285G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.732+45G>C
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8784
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

3-123471159-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471159
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471159
    reference: chr 3
allele count: 22
allele frequency: 1.818752996808915e-4
allele num: 120962
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.419+19G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.373+19G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12311G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.732+19G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.373+19G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.373+19G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.373+19G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.373+19G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2094
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

3-123471160-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471160
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471160
    reference: chr 3
allele count: 52
allele frequency: 4.298373231054093e-4
allele num: 120976
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.732+18C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.373+18C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.373+18C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.373+18C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12312C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.373+18C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.373+18C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.419+18C>T
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11665
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30275
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 9.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5886
  bin: 9.75e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2094
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-123471163-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471163
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471163
    reference: chr 3
allele count: 1
allele frequency: 8.263643275047103e-6
allele num: 121012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.373+15G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.419+15G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.373+15G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12315G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.732+15G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.373+15G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.373+15G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.373+15G>T
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11672
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8816
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP

3-123471174-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471174
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471174
    reference: chr 3
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.373+4A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.419+4A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12326A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.732+4A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.373+4A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.373+4A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.373+4A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.373+4A>G
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8836
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
hgvs: c.373+4A>G
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

3-123471174-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471174
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471174
    reference: chr 3
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.419+4A>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.373+4A>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.373+4A>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.373+4A>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12326A>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.732+4A>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.373+4A>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.373+4A>C
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: c.373+4A>C
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

3-123471178-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471178
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471178
    reference: chr 3
allele count: 2
allele frequency: 1.651118632873772e-5
allele num: 121130
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12330G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.373G>A
  hgvsp: ENSP00000352088.1:p.Gly125Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.373G>A
  hgvsp: ENSP00000418335.1:p.Gly125Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.419G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.373G>A
  hgvsp: ENSP00000320622.5:p.Gly125Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.373G>A
  hgvsp: ENSP00000353452.3:p.Gly125Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.373G>A
  hgvsp: ENSP00000354004.3:p.Gly125Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.732G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2099
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly125Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

3-123471182-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471182
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471182
    reference: chr 3
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.369A>T
  hgvsp: ENST00000360304.3:c.369A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.415A>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.369A>T
  hgvsp: ENST00000346322.5:c.369A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.369A>T
  hgvsp: ENST00000360772.3:c.369A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.369A>T
  hgvsp: ENST00000475616.1:c.369A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.728A>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.369A>T
  hgvsp: ENST00000359169.1:c.369A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12334A>T
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8848
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val123Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

3-123471183-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471183
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471183
    reference: chr 3
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.414T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.368T>C
  hgvsp: ENSP00000320622.5:p.Val123Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.368T>C
  hgvsp: ENSP00000418335.1:p.Val123Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.368T>C
  hgvsp: ENSP00000352088.1:p.Val123Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.368T>C
  hgvsp: ENSP00000353452.3:p.Val123Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12335T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.727T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.368T>C
  hgvsp: ENSP00000354004.3:p.Val123Ala
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2104
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val123Ala
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

3-123471184-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471184
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471184
    reference: chr 3
allele count: 1
allele frequency: 8.252867871585376e-6
allele num: 121170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.367G>A
  hgvsp: ENSP00000352088.1:p.Val123Ile
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12336G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.413G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.367G>A
  hgvsp: ENSP00000418335.1:p.Val123Ile
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.726G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.367G>A
  hgvsp: ENSP00000353452.3:p.Val123Ile
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.367G>A
  hgvsp: ENSP00000354004.3:p.Val123Ile
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.367G>A
  hgvsp: ENSP00000320622.5:p.Val123Ile
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5830
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2105
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val123Ile
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

3-123471185-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471185
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471185
    reference: chr 3
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.725A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.366A>G
  hgvsp: ENST00000475616.1:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.412A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.366A>G
  hgvsp: ENST00000360304.3:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.366A>G
  hgvsp: ENST00000346322.5:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.366A>G
  hgvsp: ENST00000359169.1:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.366A>G
  hgvsp: ENST00000360772.3:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12337A>G
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2105
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8853
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr122Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

3-123471186-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471186
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471186
    reference: chr 3
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.365C>T
  hgvsp: ENSP00000320622.5:p.Thr122Ile
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.365C>T
  hgvsp: ENSP00000353452.3:p.Thr122Ile
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.365C>T
  hgvsp: ENSP00000352088.1:p.Thr122Ile
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.365C>T
  hgvsp: ENSP00000418335.1:p.Thr122Ile
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.724C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.411C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12338C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.365C>T
  hgvsp: ENSP00000354004.3:p.Thr122Ile
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5828
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39901
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr122Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

3-123471195-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471195
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471195
    reference: chr 3
allele count: 2
allele frequency: 1.649702228747711e-5
allele num: 121234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12347T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.356T>C
  hgvsp: ENSP00000354004.3:p.Val119Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.356T>C
  hgvsp: ENSP00000352088.1:p.Val119Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.356T>C
  hgvsp: ENSP00000418335.1:p.Val119Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.356T>C
  hgvsp: ENSP00000353452.3:p.Val119Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.356T>C
  hgvsp: ENSP00000320622.5:p.Val119Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.402T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.715T>C
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8852
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val119Ala
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-123471196-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471196
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471196
    reference: chr 3
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.355G>A
  hgvsp: ENSP00000353452.3:p.Val119Met
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.401G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.355G>A
  hgvsp: ENSP00000418335.1:p.Val119Met
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.714G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.355G>A
  hgvsp: ENSP00000352088.1:p.Val119Met
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.355G>A
  hgvsp: ENSP00000320622.5:p.Val119Met
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12348G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.355G>A
  hgvsp: ENSP00000354004.3:p.Val119Met
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39999
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5826
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val119Met
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

3-123471207-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471207
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471207
    reference: chr 3
allele count: 14
allele frequency: 1.154505871487004e-4
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.703G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.344G>A
  hgvsp: ENSP00000418335.1:p.Arg115His
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.344G>A
  hgvsp: ENSP00000352088.1:p.Arg115His
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.390G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.344G>A
  hgvsp: ENSP00000353452.3:p.Arg115His
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.344G>A
  hgvsp: ENSP00000320622.5:p.Arg115His
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12359G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.344G>A
  hgvsp: ENSP00000354004.3:p.Arg115His
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10353
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11705
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg115His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

3-123471208-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471208
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471208
    reference: chr 3
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12360C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.343C>T
  hgvsp: ENSP00000352088.1:p.Arg115Cys
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.343C>T
  hgvsp: ENSP00000354004.3:p.Arg115Cys
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.343C>T
  hgvsp: ENSP00000353452.3:p.Arg115Cys
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.343C>T
  hgvsp: ENSP00000418335.1:p.Arg115Cys
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.343C>T
  hgvsp: ENSP00000320622.5:p.Arg115Cys
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.702C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.389C>T
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg115Cys
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

3-123471211-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471211
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471211
    reference: chr 3
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.340G>C
  hgvsp: ENSP00000353452.3:p.Ala114Pro
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.340G>C
  hgvsp: ENSP00000354004.3:p.Ala114Pro
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.699G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.386G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12363G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.340G>C
  hgvsp: ENSP00000352088.1:p.Ala114Pro
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.340G>C
  hgvsp: ENSP00000320622.5:p.Ala114Pro
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.340G>C
  hgvsp: ENSP00000418335.1:p.Ala114Pro
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2112
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8865
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala114Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-123471211-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471211
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471211
    reference: chr 3
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.340G>A
  hgvsp: ENSP00000352088.1:p.Ala114Thr
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.340G>A
  hgvsp: ENSP00000354004.3:p.Ala114Thr
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.699G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.340G>A
  hgvsp: ENSP00000353452.3:p.Ala114Thr
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12363G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.340G>A
  hgvsp: ENSP00000320622.5:p.Ala114Thr
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.340G>A
  hgvsp: ENSP00000418335.1:p.Ala114Thr
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.386G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5814
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ala114Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

3-123471227-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471227
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471227
    reference: chr 3
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.324C>T
  hgvsp: ENST00000360304.3:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.324C>T
  hgvsp: ENST00000475616.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.683C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.370C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.324C>T
  hgvsp: ENST00000360772.3:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12379C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.324C>T
  hgvsp: ENST00000346322.5:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.324C>T
  hgvsp: ENST00000359169.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2111
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8869
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala108Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

3-123471229-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471229
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471229
    reference: chr 3
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.322G>A
  hgvsp: ENSP00000418335.1:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.322G>A
  hgvsp: ENSP00000352088.1:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.368G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12381G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.322G>A
  hgvsp: ENSP00000320622.5:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.322G>A
  hgvsp: ENSP00000353452.3:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.681G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.322G>A
  hgvsp: ENSP00000354004.3:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40139
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala108Thr
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

3-123471237-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471237
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471237
    reference: chr 3
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.673C>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12389C>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.314C>A
  hgvsp: ENSP00000352088.1:p.Thr105Asn
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.314C>A
  hgvsp: ENSP00000354004.3:p.Thr105Asn
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.314C>A
  hgvsp: ENSP00000320622.5:p.Thr105Asn
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.314C>A
  hgvsp: ENSP00000353452.3:p.Thr105Asn
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.360C>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.314C>A
  hgvsp: ENSP00000418335.1:p.Thr105Asn
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr105Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-123471239-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471239
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471239
    reference: chr 3
allele count: 5
allele frequency: 4.121671750061825e-5
allele num: 121310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.312T>C
  hgvsp: ENST00000360772.3:c.312T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.312T>C
  hgvsp: ENST00000359169.1:c.312T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.312T>C
  hgvsp: ENST00000360304.3:c.312T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.671T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.312T>C
  hgvsp: ENST00000346322.5:c.312T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.358T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.312T>C
  hgvsp: ENST00000475616.1:c.312T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12391T>C
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr104Tyr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/3-123471246-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471246
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471246
    reference: chr 3
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.305G>T
  hgvsp: ENSP00000354004.3:p.Gly102Val
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.305G>T
  hgvsp: ENSP00000353452.3:p.Gly102Val
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.351G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.305G>T
  hgvsp: ENSP00000320622.5:p.Gly102Val
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.305G>T
  hgvsp: ENSP00000418335.1:p.Gly102Val
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.305G>T
  hgvsp: ENSP00000352088.1:p.Gly102Val
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12398G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.664G>T
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8862
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5808
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40105
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly102Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

3-123471246-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471246
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471246
    reference: chr 3
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.305G>A
  hgvsp: ENSP00000320622.5:p.Gly102Glu
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.664G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.305G>A
  hgvsp: ENSP00000354004.3:p.Gly102Glu
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12398G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.305G>A
  hgvsp: ENSP00000353452.3:p.Gly102Glu
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.305G>A
  hgvsp: ENSP00000352088.1:p.Gly102Glu
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.351G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.305G>A
  hgvsp: ENSP00000418335.1:p.Gly102Glu
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2105
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2099
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40105
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly102Glu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

3-123471257-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471257
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471257
    reference: chr 3
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.340G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.294G>A
  hgvsp: ENST00000359169.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.294G>A
  hgvsp: ENST00000360772.3:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.294G>A
  hgvsp: ENST00000475616.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.653G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12409G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.294G>A
  hgvsp: ENST00000360304.3:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.294G>A
  hgvsp: ENST00000346322.5:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8857
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu98Glu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum

3-123471261-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471261
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471261
    reference: chr 3
allele count: 4
allele frequency: 3.298697014679201e-5
allele num: 121260
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.290A>G
  hgvsp: ENSP00000353452.3:p.His97Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.649A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.290A>G
  hgvsp: ENSP00000418335.1:p.His97Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.290A>G
  hgvsp: ENSP00000320622.5:p.His97Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.290A>G
  hgvsp: ENSP00000354004.3:p.His97Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.336A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.290A>G
  hgvsp: ENSP00000352088.1:p.His97Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12413A>G
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2097
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His97Arg
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

3-123471262-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471262
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471262
    reference: chr 3
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.289C>T
  hgvsp: ENSP00000353452.3:p.His97Tyr
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12414C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.335C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.648C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.289C>T
  hgvsp: ENSP00000320622.5:p.His97Tyr
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.289C>T
  hgvsp: ENSP00000418335.1:p.His97Tyr
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.289C>T
  hgvsp: ENSP00000354004.3:p.His97Tyr
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.289C>T
  hgvsp: ENSP00000352088.1:p.His97Tyr
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8853
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His97Tyr
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff

3-123471263-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471263
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471263
    reference: chr 3
allele count: 4
allele frequency: 3.298588204248581e-5
allele num: 121264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.288C>G
  hgvsp: ENST00000359169.1:c.288C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.288C>G
  hgvsp: ENST00000360304.3:c.288C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.288C>G
  hgvsp: ENST00000360772.3:c.288C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.334C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.288C>G
  hgvsp: ENST00000475616.1:c.288C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.647C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.288C>G
  hgvsp: ENST00000346322.5:c.288C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12415C>G
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5799
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2105
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val96Val
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: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

3-123471271-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471271
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471271
    reference: chr 3
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.280C>G
  hgvsp: ENSP00000353452.3:p.His94Asp
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12423C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.326C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.639C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.280C>G
  hgvsp: ENSP00000320622.5:p.His94Asp
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.280C>G
  hgvsp: ENSP00000354004.3:p.His94Asp
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.280C>G
  hgvsp: ENSP00000352088.1:p.His94Asp
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.280C>G
  hgvsp: ENSP00000418335.1:p.His94Asp
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His94Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD

3-123471291-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471291
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471291
    reference: chr 3
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.260G>C
  hgvsp: ENSP00000418335.1:p.Gly87Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.260G>C
  hgvsp: ENSP00000354004.3:p.Gly87Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.619G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.260G>C
  hgvsp: ENSP00000353452.3:p.Gly87Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.260G>C
  hgvsp: ENSP00000320622.5:p.Gly87Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.260G>C
  hgvsp: ENSP00000352088.1:p.Gly87Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.306G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12443G>C
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39635
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2074
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly87Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

3-123471291-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471291
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471291
    reference: chr 3
allele count: 97
allele frequency: 8.012820512820513e-4
allele num: 121056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.306G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.260G>A
  hgvsp: ENSP00000353452.3:p.Gly87Glu
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.260G>A
  hgvsp: ENSP00000320622.5:p.Gly87Glu
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.260G>A
  hgvsp: ENSP00000352088.1:p.Gly87Glu
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12443G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.260G>A
  hgvsp: ENSP00000418335.1:p.Gly87Glu
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.260G>A
  hgvsp: ENSP00000354004.3:p.Gly87Glu
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.619G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 9.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30496
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11642
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2074
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8756
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39635
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly87Glu
num of homozygotes: 2
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ

3-123471294-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471294
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471294
    reference: chr 3
allele count: 10
allele frequency: 8.262687356435808e-5
allele num: 121026
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.257G>A
  hgvsp: ENSP00000353452.3:p.Arg86Gln
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.257G>A
  hgvsp: ENSP00000352088.1:p.Arg86Gln
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.257G>A
  hgvsp: ENSP00000320622.5:p.Arg86Gln
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.303G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.257G>A
  hgvsp: ENSP00000354004.3:p.Arg86Gln
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.257G>A
  hgvsp: ENSP00000418335.1:p.Arg86Gln
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12446G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.616G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10175
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30537
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39711
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8741
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg86Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

3-123471295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471295
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471295
    reference: chr 3
allele count: 21
allele frequency: 1.735307727903748e-4
allele num: 121016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12447C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.256C>T
  hgvsp: ENSP00000418335.1:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.256C>T
  hgvsp: ENSP00000353452.3:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.256C>T
  hgvsp: ENSP00000320622.5:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.256C>T
  hgvsp: ENSP00000352088.1:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.615C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.256C>T
  hgvsp: ENSP00000354004.3:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.302C>T
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39794
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8743
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg86Trp
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP

3-123471300-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471300
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471300
    reference: chr 3
allele count: 1
allele frequency: 8.26801600687899e-6
allele num: 120948
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.251G>C
  hgvsp: ENSP00000354004.3:p.Gly84Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.251G>C
  hgvsp: ENSP00000353452.3:p.Gly84Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.610G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12452G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.251G>C
  hgvsp: ENSP00000352088.1:p.Gly84Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.251G>C
  hgvsp: ENSP00000320622.5:p.Gly84Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.251G>C
  hgvsp: ENSP00000418335.1:p.Gly84Ala
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.297G>C
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5687
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2056
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly84Ala
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

3-123471301-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471301
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471301
    reference: chr 3
allele count: 6
allele frequency: 4.961794184777215e-5
allele num: 120924
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.250G>A
  hgvsp: ENSP00000353452.3:p.Gly84Ser
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.250G>A
  hgvsp: ENSP00000418335.1:p.Gly84Ser
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.250G>A
  hgvsp: ENSP00000320622.5:p.Gly84Ser
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.250G>A
  hgvsp: ENSP00000354004.3:p.Gly84Ser
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12453G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.609G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.296G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.250G>A
  hgvsp: ENSP00000352088.1:p.Gly84Ser
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11507
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39534
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly84Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

3-123471302-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471302
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471302
    reference: chr 3
allele count: 8
allele frequency: 6.617695718350871e-5
allele num: 120888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.249C>T
  hgvsp: ENST00000346322.5:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.249C>T
  hgvsp: ENST00000360304.3:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.249C>T
  hgvsp: ENST00000475616.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.608C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.249C>T
  hgvsp: ENST00000360772.3:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.249C>T
  hgvsp: ENST00000359169.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.295C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12454C>T
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8674
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39517
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys83Cys
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP

3-123471306-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471306
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471306
    reference: chr 3
allele count: 2
allele frequency: 1.654642928056125e-5
allele num: 120872
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.604A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.245A>G
  hgvsp: ENSP00000353452.3:p.Asp82Gly
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.245A>G
  hgvsp: ENSP00000354004.3:p.Asp82Gly
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.291A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.245A>G
  hgvsp: ENSP00000418335.1:p.Asp82Gly
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.245A>G
  hgvsp: ENSP00000320622.5:p.Asp82Gly
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.245A>G
  hgvsp: ENSP00000352088.1:p.Asp82Gly
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12458A>G
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39779
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp82Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

3-123471318-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471318
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471318
    reference: chr 3
allele count: 1
allele frequency: 8.300683976359652e-6
allele num: 120472
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.233G>A
  hgvsp: ENSP00000353452.3:p.Arg78His
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.233G>A
  hgvsp: ENSP00000352088.1:p.Arg78His
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12470G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.233G>A
  hgvsp: ENSP00000418335.1:p.Arg78His
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.279G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.233G>A
  hgvsp: ENSP00000320622.5:p.Arg78His
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.233G>A
  hgvsp: ENSP00000354004.3:p.Arg78His
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.592G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1959
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg78His
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

3-123471319-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471319
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471319
    reference: chr 3
allele count: 3
allele frequency: 2.491859924247458e-5
allele num: 120392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.591C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.278C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.232C>T
  hgvsp: ENSP00000418335.1:p.Arg78Cys
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12471C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.232C>T
  hgvsp: ENSP00000353452.3:p.Arg78Cys
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.232C>T
  hgvsp: ENSP00000354004.3:p.Arg78Cys
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.232C>T
  hgvsp: ENSP00000320622.5:p.Arg78Cys
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.232C>T
  hgvsp: ENSP00000352088.1:p.Arg78Cys
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11049
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38791
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg78Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

3-123471322-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471322
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471322
    reference: chr 3
allele count: 1
allele frequency: 8.30923654734603e-6
allele num: 120348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.229G>A
  hgvsp: ENSP00000418335.1:p.Gly77Ser
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.229G>A
  hgvsp: ENSP00000352088.1:p.Gly77Ser
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.229G>A
  hgvsp: ENSP00000353452.3:p.Gly77Ser
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.275G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.229G>A
  hgvsp: ENSP00000354004.3:p.Gly77Ser
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.588G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12474G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.229G>A
  hgvsp: ENSP00000320622.5:p.Gly77Ser
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1916
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly77Ser
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

3-123471325-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471325
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471325
    reference: chr 3
allele count: 5
allele frequency: 4.160010649627263e-5
allele num: 120192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.226G>A
  hgvsp: ENSP00000320622.5:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.226G>A
  hgvsp: ENSP00000418335.1:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.226G>A
  hgvsp: ENSP00000354004.3:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.585G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.226G>A
  hgvsp: ENSP00000353452.3:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.226G>A
  hgvsp: ENSP00000352088.1:p.Gly76Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.272G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12477G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39019
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly76Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

3-123471326-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471326
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471326
    reference: chr 3
allele count: 5
allele frequency: 4.162365555592554e-5
allele num: 120124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12478C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.225C>T
  hgvsp: ENST00000360772.3:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.225C>T
  hgvsp: ENST00000360304.3:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.225C>T
  hgvsp: ENST00000346322.5:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.271C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.584C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.225C>T
  hgvsp: ENST00000475616.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.225C>T
  hgvsp: ENST00000359169.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29744
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5602
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser75Ser
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

3-123471328-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471328
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471328
    reference: chr 3
allele count: 1
allele frequency: 8.3301401129567e-6
allele num: 120046
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.223A>G
  hgvsp: ENSP00000353452.3:p.Ser75Gly
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.582A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12480A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.223A>G
  hgvsp: ENSP00000352088.1:p.Ser75Gly
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.223A>G
  hgvsp: ENSP00000418335.1:p.Ser75Gly
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.223A>G
  hgvsp: ENSP00000354004.3:p.Ser75Gly
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.223A>G
  hgvsp: ENSP00000320622.5:p.Ser75Gly
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.269A>G
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29683
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39060
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8336
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser75Gly
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

3-123471332-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471332
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471332
    reference: chr 3
allele count: 1
allele frequency: 8.342231713828083e-6
allele num: 119872
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.219C>G
  hgvsp: ENSP00000418335.1:p.Ile73Met
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.578C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.265C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.219C>G
  hgvsp: ENSP00000320622.5:p.Ile73Met
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12484C>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.219C>G
  hgvsp: ENSP00000354004.3:p.Ile73Met
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.219C>G
  hgvsp: ENSP00000352088.1:p.Ile73Met
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.219C>G
  hgvsp: ENSP00000353452.3:p.Ile73Met
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5588
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8246
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile73Met
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS

3-123471335-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471335
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471335
    reference: chr 3
allele count: 1
allele frequency: 8.35812911637859e-6
allele num: 119644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.216C>T
  hgvsp: ENST00000359169.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.262C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.575C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.216C>T
  hgvsp: ENST00000360304.3:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.216C>T
  hgvsp: ENST00000360772.3:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.216C>T
  hgvsp: ENST00000346322.5:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12487C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.216C>T
  hgvsp: ENST00000475616.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1849
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro72Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

3-123471341-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471341
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471341
    reference: chr 3
allele count: 1
allele frequency: 8.389965601141035e-6
allele num: 119190
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12493G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.210G>A
  hgvsp: ENST00000359169.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.210G>A
  hgvsp: ENST00000360304.3:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.210G>A
  hgvsp: ENST00000475616.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.569G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.210G>A
  hgvsp: ENST00000360772.3:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.210G>A
  hgvsp: ENST00000346322.5:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.256G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10249
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5564
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2097
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly70Gly
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

3-123471343-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471343
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471343
    reference: chr 3
allele count: 1
allele frequency: 8.411277841329655e-6
allele num: 118888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.208G>A
  hgvsp: ENSP00000352088.1:p.Gly70Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12495G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.208G>A
  hgvsp: ENSP00000320622.5:p.Gly70Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.567G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.208G>A
  hgvsp: ENSP00000418335.1:p.Gly70Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.208G>A
  hgvsp: ENSP00000354004.3:p.Gly70Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.254G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.208G>A
  hgvsp: ENSP00000353452.3:p.Gly70Arg
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5546
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly70Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD

3-123471344-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471344
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471344
    reference: chr 3
allele count: 41
allele frequency: 3.447579967037772e-4
allele num: 118924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12496C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.253C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.207C>T
  hgvsp: ENST00000346322.5:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.207C>T
  hgvsp: ENST00000359169.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.207C>T
  hgvsp: ENST00000360772.3:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.207C>T
  hgvsp: ENST00000360304.3:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.566C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.207C>T
  hgvsp: ENST00000475616.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11606
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10050
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28693
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1569
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn69Asn
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

3-123471361-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471361
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471361
    reference: chr 3
allele count: 2
allele frequency: 1.7361412524523e-5
allele num: 115198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.190G>A
  hgvsp: ENSP00000352088.1:p.Val64Met
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.190G>A
  hgvsp: ENSP00000353452.3:p.Val64Met
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.236G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.190G>A
  hgvsp: ENSP00000418335.1:p.Val64Met
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.549G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.190G>A
  hgvsp: ENSP00000354004.3:p.Val64Met
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.190G>A
  hgvsp: ENSP00000320622.5:p.Val64Met
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12513G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9065
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5512
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35410
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7235
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1409
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val64Met
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

3-123471363-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471363
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471363
    reference: chr 3
allele count: 2
allele frequency: 1.75960303355563e-5
allele num: 113662
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12515A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.188A>G
  hgvsp: ENSP00000352088.1:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.188A>G
  hgvsp: ENSP00000320622.5:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.547A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.188A>G
  hgvsp: ENSP00000418335.1:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.188A>G
  hgvsp: ENSP00000354004.3:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.188A>G
  hgvsp: ENSP00000353452.3:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.234A>G
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8744
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5507
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln63Arg
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

3-123471371-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471371
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471371
    reference: chr 3
allele count: 1
allele frequency: 9.067827348567284e-6
allele num: 110280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.180A>G
  hgvsp: ENST00000360772.3:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12523A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.539A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.180A>G
  hgvsp: ENST00000359169.1:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.226A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.180A>G
  hgvsp: ENST00000346322.5:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.180A>G
  hgvsp: ENST00000360304.3:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.180A>G
  hgvsp: ENST00000475616.1:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11861
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5494
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30950
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro60Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

3-123471381-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471381
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471381
    reference: chr 3
allele count: 3
allele frequency: 3.056732963808281e-5
allele num: 98144
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.529G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.170G>A
  hgvsp: ENSP00000352088.1:p.Arg57Gln
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.170G>A
  hgvsp: ENSP00000353452.3:p.Arg57Gln
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.170G>A
  hgvsp: ENSP00000418335.1:p.Arg57Gln
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.170G>A
  hgvsp: ENSP00000354004.3:p.Arg57Gln
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.170G>A
  hgvsp: ENSP00000320622.5:p.Arg57Gln
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.216G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12533G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14592
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19800
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22331
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg57Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

3-123471382-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471382
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471382
    reference: chr 3
allele count: 1
allele frequency: 1.046725841567577e-5
allele num: 95536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.215C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12534C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.169C>T
  hgvsp: ENSP00000353452.3:p.Arg57Trp
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.169C>T
  hgvsp: ENSP00000320622.5:p.Arg57Trp
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.169C>T
  hgvsp: ENSP00000352088.1:p.Arg57Trp
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.169C>T
  hgvsp: ENSP00000418335.1:p.Arg57Trp
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.528C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.169C>T
  hgvsp: ENSP00000354004.3:p.Arg57Trp
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13013
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24392
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3191
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2223
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg57Trp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/3-123471385-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471385
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471385
    reference: chr 3
allele count: 1
allele frequency: 1.071375002678437e-5
allele num: 93338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12537G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.166G>T
  hgvsp: ENSP00000353452.3:p.Val56Phe
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.166G>T
  hgvsp: ENSP00000352088.1:p.Val56Phe
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.166G>T
  hgvsp: ENSP00000320622.5:p.Val56Phe
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.525G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.166G>T
  hgvsp: ENSP00000354004.3:p.Val56Phe
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.166G>T
  hgvsp: ENSP00000418335.1:p.Val56Phe
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.212G>T
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4924
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2981
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15168
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2398
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val56Phe
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: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD

3-123471392-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471392
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471391
    reference: chr 3
allele count: 3
allele frequency: 3.60915281153004e-5
allele num: 83122
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.166-8delT
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.166-8delT
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.212-8delT
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.166-8delT
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.166-8delT
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.525-8delT
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.166-8delT
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12545delT
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22470
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3221
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7229
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2604
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31644
  bin: 2.25e1
  variant carriers: 0
hgvs: c.166-8delT
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: GA
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

3-123471408-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471408
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471408
    reference: chr 3
allele count: 1
allele frequency: 1.504257047444267e-5
allele num: 66478
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.166-23A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.166-23A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.166-23A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.212-23A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.525-23A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12560A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.166-23A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.166-23A>G
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19975
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21757
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6389
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6974
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1866
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29682
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD

3-123471424-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471424
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471424
    reference: chr 3
allele count: 1
allele frequency: 1.882317509317472e-5
allele num: 53126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.166-39T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.212-39T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.166-39T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12576T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.166-39T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.525-39T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.166-39T>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.166-39T>C
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4536
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3875
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23002
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10536
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

3-123471426-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471426
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471426
    reference: chr 3
allele count: 3
allele frequency: 5.817561278312131e-5
allele num: 51568
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.525-41C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.166-41C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.166-41C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.212-41C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.166-41C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.166-41C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12578C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.166-41C>T
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15588
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10764
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4495
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3815
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

3-123471430-ACT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123471430
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123471428
    reference: chr 3
allele count: 1
allele frequency: 2.086375964948884e-5
allele num: 47930
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.166-47_166-46delAG
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.166-47_166-46delAG
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.212-47_212-46delAG
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.166-47_166-46delAG
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.166-47_166-46delAG
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.525-47_525-46delAG
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.166-47_166-46delAG
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.166-12584_166-12583delAG
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25944
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3653
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1483
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: ACT
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

3-123512473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123512473
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123512473
    reference: chr 3
allele count: 1
allele frequency: 8.38208915190022e-6
allele num: 119302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.165+51C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.165+51C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.524+51C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.211+51C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.165+51C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.165+51C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.165+51C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.165+51C>T
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3328
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1752
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1729
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1737
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17834
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

3-123512476-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123512476
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123512476
    reference: chr 3
allele count: 1
allele frequency: 8.366940544520491e-6
allele num: 119518
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.165+48G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.165+48G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.165+48G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.165+48G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.524+48G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.165+48G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.165+48G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.211+48G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14607
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6897
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17545
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4192
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4576
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3327
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8230
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

3-123512477-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123512477
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123512477
    reference: chr 3
allele count: 2
allele frequency: 1.672156915204923e-5
allele num: 119606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.165+47G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.165+47G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.524+47G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.165+47G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.165+47G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.165+47G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.211+47G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.165+47G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17705
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4188
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2963
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3335
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1372
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1675
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

3-123512480-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123512480
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123512480
    reference: chr 3
allele count: 1
allele frequency: 8.362882183715796e-6
allele num: 119576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.211+44C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.165+44C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.165+44C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.165+44C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.165+44C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.524+44C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.165+44C>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.165+44C>T
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1242
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23225
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3329
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1618
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8370
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ

3-123512481-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123512481
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123512481
    reference: chr 3
allele count: 1
allele frequency: 8.364421098415779e-6
allele num: 119554
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.165+43G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.211+43G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.165+43G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.165+43G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.524+43G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.165+43G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.165+43G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.165+43G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1934
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1456
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1351
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

3-123512485-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123512485
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123512485
    reference: chr 3
allele count: 1
allele frequency: 8.3462700519138e-6
allele num: 119814
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.165+39A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.211+39A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.165+39A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.524+39A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.165+39A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.165+39A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.165+39A>G
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.165+39A>G
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16923
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25327
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4601
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

3-123512486-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123512486
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123512486
    reference: chr 3
allele count: 1
allele frequency: 8.345852111500584e-6
allele num: 119820
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.211+38G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.165+38G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.165+38G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.165+38G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.165+38G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.524+38G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.165+38G>C
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.165+38G>C
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1351
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3065
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8675
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3436
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/3-123512487-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123512487
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123512487
    reference: chr 3
allele count: 6
allele frequency: 5.006341365729925e-5
allele num: 119848
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.165+37G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.165+37G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.211+37G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.524+37G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.165+37G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.165+37G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.165+37G>T
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.165+37G>T
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18873
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4072
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1736
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25938
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8711
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

3-123512493-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123512493
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123512493
    reference: chr 3
allele count: 3
allele frequency: 2.500500100020004e-5
allele num: 119976
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.165+31G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.165+31G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.211+31G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.165+31G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.165+31G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.524+31G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.165+31G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.165+31G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19445
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4312
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8842
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1782
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

3-123512499-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123512499
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 123512499
    reference: chr 3
allele count: 1
allele frequency: 8.319329129299013e-6
allele num: 120202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000354004
  ensembl transcript: ENST00000360772
  gene symbol: MYLK
  hgvsc: ENST00000360772.3:c.165+25G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000506361
  gene symbol: MYLK
  hgvsc: ENST00000506361.1:n.524+25G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000417798
  ensembl transcript: ENST00000464489
  gene symbol: MYLK
  hgvsc: ENST00000464489.1:c.165+25G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000320622
  ensembl transcript: ENST00000346322
  gene symbol: MYLK
  hgvsc: ENST00000346322.5:c.165+25G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000353452
  ensembl transcript: ENST00000360304
  gene symbol: MYLK
  hgvsc: ENST00000360304.3:c.165+25G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl transcript: ENST00000510571
  gene symbol: MYLK
  hgvsc: ENST00000510571.1:n.211+25G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000418335
  ensembl transcript: ENST00000475616
  gene symbol: MYLK
  hgvsc: ENST00000475616.1:c.165+25G>A
  variant of: http://identifiers.org/hgnc/7590
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065534
  ensembl protein: ENSP00000352088
  ensembl transcript: ENST00000359169
  gene symbol: MYLK
  hgvsc: ENST00000359169.1:c.165+25G>A
  variant of: http://identifiers.org/hgnc/7590
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8794
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5908
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 288
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2109
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.72951936174353e-5
allele num: 10278
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66368
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
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: 6612
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 2.703e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e0

QD
type: SiteQuality
SIO_000300: 1.32e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.0e-1

DP
type: SiteQuality
SIO_000300: 1.890138e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2109
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2102
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8794
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5908
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66368
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
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: 11570
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.890138e6

QD
type: SiteQuality
SIO_000300: 1.32e1

VQSLOD
type: SiteQuality
SIO_000300: 6.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 2.703e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

GenotypeQuality
all individuals: 2095
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2104
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5898
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 206
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38804
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66376
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: -2.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.414e1

FS
type: SiteQuality
SIO_000300: 4.458e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.06e-1

DP
type: SiteQuality
SIO_000300: 1.890593e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e-1

GenotypeQuality
all individuals: 5894
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 320
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8792
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39280
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
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: 66434
num of homozygotes: 0

South Asian
type: Population
allele count: 22
allele frequency: 1.332848661092936e-3
allele num: 16506
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.18e-1

DP
type: SiteQuality
SIO_000300: 1.896456e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.251e0

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.19e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

QD
type: SiteQuality
SIO_000300: 1.301e1

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8803
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39346
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 49
allele frequency: 7.375075255869958e-4
allele num: 66440
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: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.708737864077671e-5
allele num: 10300
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 6.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

QD
type: SiteQuality
SIO_000300: 1.295e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.44e0

DP
type: SiteQuality
SIO_000300: 1.898173e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.85e-1

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

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 116
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39547
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2098
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5837
bin: 9.75e1
variant carriers: 1

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: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
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: 8636
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: 1.504845602841149e-5
allele num: 66452
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.828e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.78e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.14e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

VQSLOD
type: SiteQuality
SIO_000300: 4.28e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.894633e6

GenotypeQuality
all individuals: 99
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5836
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 39786
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2100
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 8.25e1
variant carriers: 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: 8640
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
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: 1.503397678753984e-5
allele num: 66516
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: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

QD
type: SiteQuality
SIO_000300: 1.22e1

DP
type: SiteQuality
SIO_000300: 1.897422e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 3.973e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

GenotypeQuality
all individuals: 8836
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 319
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 220
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5836
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2104
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2100
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39786
bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 66516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
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: 11574
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.23e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

DP
type: SiteQuality
SIO_000300: 1.897422e6

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 3.973e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

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

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

GenotypeQuality
all individuals: 319
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 5834
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 39772
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8849
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 866
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

Latino
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South Asian
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African
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InbreedingCoeff
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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MQ
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QD
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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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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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South Asian
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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VQSLOD
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ClippingRankSum
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MQRankSum
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QD
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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QD
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MQRankSum
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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African
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Other
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European (Finnish)
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South Asian
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DP
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VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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MQ
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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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European (Non-Finnish)
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African
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South Asian
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East Asian
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European (Finnish)
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Finnish)
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Other
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African
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BaseQRankSum
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FS
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QD
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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East Asian
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African
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South Asian
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European (Non-Finnish)
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European (Finnish)
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QD
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VQSLOD
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DP
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MQ
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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VQSLOD
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DP
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InbreedingCoeff
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MQ
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FS
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African
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East Asian
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DP
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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African
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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ClippingRankSum
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VQSLOD
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MQ
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FS
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ReadPosRankSum
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MQRankSum
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DP
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InbreedingCoeff
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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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East Asian
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allele frequency: 1.156871818602499e-4
allele num: 8644
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
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QD
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FS
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MQ
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ReadPosRankSum
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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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South Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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Latino
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East Asian
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African
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BaseQRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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VQSLOD
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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East Asian
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African
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Latino
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Other
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European (Finnish)
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allele frequency: 0.0e0
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FS
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InbreedingCoeff
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ClippingRankSum
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DP
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MQRankSum
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VQSLOD
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QD
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BaseQRankSum
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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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African
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num of homozygotes: 0

Other
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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QD
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MQ
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MQRankSum
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ClippingRankSum
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VQSLOD
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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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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European (Non-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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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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InbreedingCoeff
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FS
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DP
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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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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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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Other
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DP
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MQRankSum
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BaseQRankSum
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MQ
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QD
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VQSLOD
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FS
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ReadPosRankSum
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InbreedingCoeff
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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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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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Other
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African
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European (Finnish)
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MQRankSum
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FS
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MQ
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ClippingRankSum
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QD
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DP
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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MQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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FS
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DP
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ClippingRankSum
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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
all individuals: 287
bin: 8.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.34e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.311e1

MQ
type: SiteQuality
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VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.4518e1

DP
type: SiteQuality
SIO_000300: 1.90028e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.67e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001380635092142e-5
allele num: 66636
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: 5.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.51e-1

QD
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MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

DP
type: SiteQuality
SIO_000300: 1.900301e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

VQSLOD
type: SiteQuality
SIO_000300: 9.5e-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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bin: 1.75e1
variant carriers: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 8628
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: 7.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.49e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.765e0

FS
type: SiteQuality
SIO_000300: 4.472e0

DP
type: SiteQuality
SIO_000300: 1.899914e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.900034e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.83e-1

FS
type: SiteQuality
SIO_000300: 5.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 9.24e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.327e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 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: 908
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.213e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.898834e6

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

QD
type: SiteQuality
SIO_000300: 1.317e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 311
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66520
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
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: 908
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.38e-1

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.98e-2

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.917e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.274e1

DP
type: SiteQuality
SIO_000300: 1.897114e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
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allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 95
allele frequency: 5.756877954187371e-3
allele num: 16502
num of homozygotes: 2

Latino
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allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66520
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
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VQSLOD
type: SiteQuality
SIO_000300: 3.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.836e0

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.38e-1

DP
type: SiteQuality
SIO_000300: 1.897114e6

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.976e1

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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African
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allele count: 3
allele frequency: 2.897990726429675e-4
allele num: 10352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.052473312283867e-4
allele num: 66510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.890125e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

FS
type: SiteQuality
SIO_000300: 5.639999999999999e-1

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
type: Population
allele count: 12
allele frequency: 1.393081030879963e-3
allele num: 8614
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.732801940738174e-4
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.511006856730422e-5
allele num: 66504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 2
allele frequency: 1.932367149758454e-4
allele num: 10350
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South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.375e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

DP
type: SiteQuality
SIO_000300: 1.889406e6

GenotypeQuality
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GenotypeQuality
all individuals: 63
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8730
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2047
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504619180885318e-5
allele num: 66462
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.879999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.88549e6

FS
type: SiteQuality
SIO_000300: 6.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e0

QD
type: SiteQuality
SIO_000300: 1.357e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2048
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.515080368430558e-5
allele num: 66444
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.818622696411251e-4
allele num: 16496
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-1

FS
type: SiteQuality
SIO_000300: 4.371e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.16e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.023e0

DP
type: SiteQuality
SIO_000300: 1.884494e6

QD
type: SiteQuality
SIO_000300: 1.451e1

GenotypeQuality
all individuals: 118
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5652
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variant carriers: 8

GenotypeQuality
all individuals: 2031
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 5.801585766776252e-4
allele num: 10342
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66426
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.94e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.412e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

QD
type: SiteQuality
SIO_000300: 1.288e1

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

DP
type: SiteQuality
SIO_000300: 1.883772e6

GenotypeQuality
all individuals: 817
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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variant carriers: 2

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66416
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.934235976789168e-4
allele num: 10340
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.808e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.406e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.1e0

QD
type: SiteQuality
SIO_000300: 1.128e1

FS
type: SiteQuality
SIO_000300: 1.262e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.59e-1

DP
type: SiteQuality
SIO_000300: 1.880717e6

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1984
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GenotypeQuality
all individuals: 5624
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39047
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.720062208398134e-5
allele num: 10288
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66194
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.473e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.868314e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.17e-1

GenotypeQuality
all individuals: 221
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
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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: 346
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GenotypeQuality
all individuals: 272
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GenotypeQuality
all individuals: 5622
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1970
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511532996765319e-5
allele num: 66158
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.194e1

MQRankSum
type: SiteQuality
SIO_000300: -3.27e-1

FS
type: SiteQuality
SIO_000300: 1.168e0

VQSLOD
type: SiteQuality
SIO_000300: 6.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.71e-1

DP
type: SiteQuality
SIO_000300: 1.86487e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

GenotypeQuality
all individuals: 18
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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: 136
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GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.045e0

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.862073e6

VQSLOD
type: SiteQuality
SIO_000300: 2.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.956e1

QD
type: SiteQuality
SIO_000300: 7.28e0

GenotypeQuality
all individuals: 289
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
all individuals: 24
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1090
bin: 2.25e1
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GenotypeQuality
all individuals: 157
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.744689144416293e-5
allele num: 10262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.0549181072326e-5
allele num: 66062
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.695e1

VQSLOD
type: SiteQuality
SIO_000300: 9.67e-1

FS
type: SiteQuality
SIO_000300: 3.221e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-1

DP
type: SiteQuality
SIO_000300: 1.858661e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.046e0

GenotypeQuality
all individuals: 8333
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1160
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GenotypeQuality
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GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 38911
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GenotypeQuality
all individuals: 292
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GenotypeQuality
all individuals: 1866
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GenotypeQuality
all individuals: 223
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GenotypeQuality
all individuals: 765
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GenotypeQuality
all individuals: 234
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variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21654501216545e-4
allele num: 16440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
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European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.543389368468878e-5
allele num: 66030
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

DP
type: SiteQuality
SIO_000300: 1.855897e6

MQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.179e0

FS
type: SiteQuality
SIO_000300: 3.994e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.275e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 1860
bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 252
bin: 5.25e1
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GenotypeQuality
all individuals: 763
bin: 8.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.171234481143125e-4
allele num: 8538
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65992
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.874e1

QD
type: SiteQuality
SIO_000300: 8.82e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.55e0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.016e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.539e0

DP
type: SiteQuality
SIO_000300: 1.852721e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
all individuals: 10
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65904
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.090875867949811e-5
allele num: 16418
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-1

QD
type: SiteQuality
SIO_000300: 1.174e1

MQ
type: SiteQuality
SIO_000300: 5.876e1

VQSLOD
type: SiteQuality
SIO_000300: -1.223e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 4.691e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52077376969402e-5
allele num: 65756
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 4.59e0

QD
type: SiteQuality
SIO_000300: 1.363e1

VQSLOD
type: SiteQuality
SIO_000300: 7.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.03e-1

DP
type: SiteQuality
SIO_000300: 1.843596e6

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526251526251526e-5
allele num: 65520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.203e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.092e0

QD
type: SiteQuality
SIO_000300: 1.124e1

DP
type: SiteQuality
SIO_000300: 1.831113e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: 6.94e-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
all individuals: 200
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GenotypeQuality
all individuals: 38452
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529940944279551e-5
allele num: 65362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16338
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

VQSLOD
type: SiteQuality
SIO_000300: 2.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.824661e6

MQRankSum
type: SiteQuality
SIO_000300: -1.88e-1

QD
type: SiteQuality
SIO_000300: 1.168e1

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: 41

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 166
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variant carriers: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.163217827843761e-3
allele num: 16334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.18427285646613e-4
allele num: 8444
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.899029895070283e-5
allele num: 10102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.566416040100251e-4
allele num: 6384
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.787346221441125e-5
allele num: 11380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.752630291167115e-4
allele num: 65392
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.919e0

DP
type: SiteQuality
SIO_000300: 1.82363e6

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.988e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6116
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63414
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.249375312343828e-4
allele num: 16008
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Latino
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
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Other
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.387e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.740586e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 4.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

QD
type: SiteQuality
SIO_000300: 1.439e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.592e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10794
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6012
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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South Asian
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allele count: 2
allele frequency: 1.261670451678022e-4
allele num: 15852
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.14e-1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.67e-1

FS
type: SiteQuality
SIO_000300: 6.38e-1

DP
type: SiteQuality
SIO_000300: 1.709235e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.778e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 160
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
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East Asian
type: Population
allele count: 1
allele frequency: 1.294665976178146e-4
allele num: 7724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60782
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.665e1

VQSLOD
type: SiteQuality
SIO_000300: -1.224e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.933e0

ClippingRankSum
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SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 1.63666e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.776e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.5e-1

GenotypeQuality
all individuals: 273
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2522
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 734
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5491
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 248
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3633
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8890
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.848376934666484e-5
allele num: 14602
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.489425081918379e-4
allele num: 6714
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.233045622688039e-4
allele num: 8110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

QD
type: SiteQuality
SIO_000300: 2.332e1

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

FS
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.399884e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 495
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 89
bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2815
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17073
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.264862130027827e-4
allele num: 7906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52276
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14388
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5140
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.97e-1

DP
type: SiteQuality
SIO_000300: 1.345859e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.134e0

FS
type: SiteQuality
SIO_000300: 2.381e0

MQRankSum
type: SiteQuality
SIO_000300: -4.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

QD
type: SiteQuality
SIO_000300: 1.129e1

GenotypeQuality
all individuals: 155
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
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variant carriers: 0

GenotypeQuality
all individuals: 1150
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 475
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variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4976
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.960399921584003e-5
allele num: 51010
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7754
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.225e0

DP
type: SiteQuality
SIO_000300: 1.297104e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-1

QD
type: SiteQuality
SIO_000300: 1.602e1

GenotypeQuality
all individuals: 645
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5486
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 167
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1229
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variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13330
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6960
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7210
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.519756838905775e-3
allele num: 658
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.434983147064041e-5
allele num: 45096
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.117748e6

QD
type: SiteQuality
SIO_000300: 1.095e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.58e0

GenotypeQuality
all individuals: 3891
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
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variant carriers: 0

GenotypeQuality
all individuals: 177
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GenotypeQuality
all individuals: 150
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 226
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2229
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 201
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11950
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.816425392891342e-5
allele num: 35506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 540
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.88e-1

DP
type: SiteQuality
SIO_000300: 9.51143e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.46e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

QD
type: SiteQuality
SIO_000300: 7.38e0

GenotypeQuality
all individuals: 152
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3845
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3790
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5484
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3000
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4618
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.29022668153103e-5
allele num: 10764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3782
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 436
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.04e-2

QD
type: SiteQuality
SIO_000300: 1.219e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

DP
type: SiteQuality
SIO_000300: 8.73154e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.51e-1

GenotypeQuality
all individuals: 21488
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
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variant carriers: 0

GenotypeQuality
all individuals: 275
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GenotypeQuality
all individuals: 147
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 1482
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5486
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
all individuals: 5000
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3761
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.401924500370096e-5
allele num: 27020
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.494060097833683e-4
allele num: 2862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10648
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2542
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.66216e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.18e-2

QD
type: SiteQuality
SIO_000300: 1.119e1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.309e0

VQSLOD
type: SiteQuality
SIO_000300: -2.292e-1

GenotypeQuality
all individuals: 6119
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
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variant carriers: 0

GenotypeQuality
all individuals: 1670
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5484
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 247
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GenotypeQuality
all individuals: 511
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3611
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17623
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24872
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2612
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.386634844868735e-4
allele num: 4190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3192
num of homozygotes: 0

South Asian
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: 394
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.16e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 8.55752e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.555e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.573e1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.51e-2

GenotypeQuality
all individuals: 8114
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
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variant carriers: 0

GenotypeQuality
all individuals: 4256
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variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4587
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variant carriers: 1

GenotypeQuality
all individuals: 2884
bin: 4.75e1
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GenotypeQuality
all individuals: 3058
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.538461538461539e-4
allele num: 6500
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16146
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 1.590334e6

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.688e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: 8.99e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.417e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.26e-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
all individuals: 1520
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variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10066
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.179705846001731e-5
allele num: 16182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65854
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.271e0

DP
type: SiteQuality
SIO_000300: 1.59617e6

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

QD
type: SiteQuality
SIO_000300: 1.359e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.175889328063241e-5
allele num: 16192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65890
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.910802775024777e-5
allele num: 10090
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8544
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VQSLOD
type: SiteQuality
SIO_000300: 8.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQ
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DP
type: SiteQuality
SIO_000300: 1.599713e6

QD
type: SiteQuality
SIO_000300: 1.332e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65850
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16200
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.906875371507826e-5
allele num: 10094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.156e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.611523e6

FS
type: SiteQuality
SIO_000300: 4.523e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.53e-1

QD
type: SiteQuality
SIO_000300: 1.544e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1024
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518649009840846e-5
allele num: 65848
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16190
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.913e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.219e0

VQSLOD
type: SiteQuality
SIO_000300: -1.361e0

FS
type: SiteQuality
SIO_000300: 1.148e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.83e-1

DP
type: SiteQuality
SIO_000300: 1.615116e6

QD
type: SiteQuality
SIO_000300: 2.766e1

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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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.8833761612967e-5
allele num: 10118
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65968
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16240
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.630069e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.735e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.522e1

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e0

VQSLOD
type: SiteQuality
SIO_000300: 2.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

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
all individuals: 69
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GenotypeQuality
all individuals: 1735
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10114
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515564851019975e-5
allele num: 65982
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.633686e6

QD
type: SiteQuality
SIO_000300: 1.48e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.572e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e0

VQSLOD
type: SiteQuality
SIO_000300: 8.169999999999999e-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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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1409
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.610057421263268e-4
allele num: 11494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.546281142025823e-5
allele num: 65988
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10114
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.89e-1

FS
type: SiteQuality
SIO_000300: 5.32e-1

QD
type: SiteQuality
SIO_000300: 1.211e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.933e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.854e0

MQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

DP
type: SiteQuality
SIO_000300: 1.63734e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.49e-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
all individuals: 4640
bin: 9.75e1
variant carriers: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.964426877470356e-4
allele num: 10120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.73e-1

FS
type: SiteQuality
SIO_000300: 5.181e0

MQRankSum
type: SiteQuality
SIO_000300: -4.92e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.313e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-1

DP
type: SiteQuality
SIO_000300: 1.656309e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.096e0