6-39895263-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895263
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895263
    reference: chr 6
allele count: 277
allele frequency: 2.618989089121268e-3
allele num: 105766
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.55G>A
  hgvsp: ENSP00000362282.4:p.Gly19Ser
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-69G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.36+19G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-69G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.55G>A
  hgvsp: ENSP00000416478.2:p.Gly19Ser
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1674G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-69G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-69G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.36+19G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1674G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-69G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 8493
  bin: 2.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 25431
  bin: 2.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10425
  bin: 1.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 1.75e1
  variant carriers: 68
genotype quality: GenotypeQuality
hgvs: p.Gly19Ser
num of homozygotes: 1
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/6-39895263-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895263
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895263
    reference: chr 6
allele count: 1
allele frequency: 9.454834256755479e-6
allele num: 105766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1674G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.55G>T
  hgvsp: ENSP00000362282.4:p.Gly19Cys
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-69G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1674G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-69G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-69G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.55G>T
  hgvsp: ENSP00000416478.2:p.Gly19Cys
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.36+19G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-69G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.36+19G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-69G>T
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly19Cys
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

6-39895264-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895264
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895264
    reference: chr 6
allele count: 3
allele frequency: 2.834734952281962e-5
allele num: 105830
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-70C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.54C>T
  hgvsp: ENST00000373186.4:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-70C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1675C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1675C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.54C>T
  hgvsp: ENST00000425303.2:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.36+18C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.36+18C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-70C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-70C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-70C>T
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5237
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10086
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26031
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly18Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

6-39895264-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895264
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895264
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 105830
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.36+18C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-70C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.54C>A
  hgvsp: ENST00000373186.4:c.54C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1675C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.36+18C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-70C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.54C>A
  hgvsp: ENST00000425303.2:c.54C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-70C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1675C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-70C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-70C>A
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10086
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly18Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

6-39895268-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895268
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895268
    reference: chr 6
allele count: 1
allele frequency: 9.379455241239589e-6
allele num: 106616
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1679C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-74C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.50C>A
  hgvsp: ENSP00000362282.4:p.Ala17Glu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-74C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.36+14C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.36+14C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1679C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-74C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.50C>A
  hgvsp: ENSP00000416478.2:p.Ala17Glu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-74C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-74C>A
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala17Glu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

6-39895269-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895269
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895269
    reference: chr 6
allele count: 1
allele frequency: 9.375585974123383e-6
allele num: 106660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-75G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1680G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-75G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-75G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1680G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-75G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.49G>A
  hgvsp: ENSP00000362282.4:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-75G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.49G>A
  hgvsp: ENSP00000416478.2:p.Ala17Thr
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.36+13G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.36+13G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4536
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala17Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-39895272-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895272
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895272
    reference: chr 6
allele count: 1
allele frequency: 9.322618537094698e-6
allele num: 107266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.36+10G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.46G>A
  hgvsp: ENSP00000416478.2:p.Gly16Arg
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-78G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.36+10G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-78G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-78G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.46G>A
  hgvsp: ENSP00000362282.4:p.Gly16Arg
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-78G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-78G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1683G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1683G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly16Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

6-39895276-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895276
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895276
    reference: chr 6
allele count: 1
allele frequency: 9.2910898448388e-6
allele num: 107630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1687G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.36+6G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-82G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.42G>C
  hgvsp: ENSP00000362282.4:p.Arg14Ser
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-82G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-82G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.42G>C
  hgvsp: ENSP00000416478.2:p.Arg14Ser
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1687G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-82G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-82G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.36+6G>C
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8380
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg14Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

6-39895278-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895278
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895278
    reference: chr 6
allele count: 3
allele frequency: 2.784016035932367e-5
allele num: 107758
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-84A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-84A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.36+4A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.40A>G
  hgvsp: ENSP00000362282.4:p.Arg14Gly
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-84A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-84A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.40A>G
  hgvsp: ENSP00000416478.2:p.Arg14Gly
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.36+4A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1689A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-84A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1689A>G
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9612
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6026
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg14Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

6-39895281-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895281
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895281
    reference: chr 6
allele count: 3
allele frequency: 2.77808645405045e-5
allele num: 107988
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.36+1G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.37G>A
  hgvsp: ENSP00000362282.4:p.Val13Ile
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-87G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.36+1G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-87G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1692G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-87G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.37G>A
  hgvsp: ENSP00000416478.2:p.Val13Ile
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-87G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1692G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-87G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9726
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.36+1G>A
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: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-39895290-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895290
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895290
    reference: chr 6
allele count: 8
allele frequency: 7.367975096244175e-5
allele num: 108578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-96G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.28G>T
  hgvsp: ENSP00000362270.4:p.Asp10Tyr
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-96G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.28G>T
  hgvsp: ENSP00000362282.4:p.Asp10Tyr
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-96G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1701G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-96G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.28G>T
  hgvsp: ENSP00000410809.2:p.Asp10Tyr
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.28G>T
  hgvsp: ENSP00000416478.2:p.Asp10Tyr
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1701G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-96G>T
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6968
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10258
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp10Tyr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-39895291-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895291
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895290
    reference: chr 6
allele count: 1
allele frequency: 9.201494322678003e-6
allele num: 108678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.26delC
  hgvsp: ENSP00000362270.4:p.Thr9LysfsTer58
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-98delC
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1703delC
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1703delC
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.26delC
  hgvsp: ENSP00000410809.2:p.Thr9LysfsTer58
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-98delC
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-98delC
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.26delC
  hgvsp: ENSP00000416478.2:p.Thr9LysfsTer5
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-98delC
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-98delC
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.26delC
  hgvsp: ENSP00000362282.4:p.Thr9LysfsTer5
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6883
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr9LysfsTer5
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: TG
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum

6-39895295-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895295
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895295
    reference: chr 6
allele count: 2
allele frequency: 1.840129545119977e-5
allele num: 108688
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.23G>A
  hgvsp: ENSP00000416478.2:p.Arg8His
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-101G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-101G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.23G>A
  hgvsp: ENSP00000362282.4:p.Arg8His
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.23G>A
  hgvsp: ENSP00000362270.4:p.Arg8His
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-101G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.23G>A
  hgvsp: ENSP00000410809.2:p.Arg8His
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-101G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1706G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-101G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1706G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10508
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg8His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

6-39895296-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895296
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895296
    reference: chr 6
allele count: 1
allele frequency: 9.196924548431005e-6
allele num: 108732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.22C>T
  hgvsp: ENSP00000362270.4:p.Arg8Cys
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-102C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.22C>T
  hgvsp: ENSP00000416478.2:p.Arg8Cys
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.22C>T
  hgvsp: ENSP00000410809.2:p.Arg8Cys
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1707C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-102C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1707C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-102C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.22C>T
  hgvsp: ENSP00000362282.4:p.Arg8Cys
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-102C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-102C>T
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6563
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg8Cys
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

6-39895311-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895311
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895311
    reference: chr 6
allele count: 1
allele frequency: 9.153820804803925e-6
allele num: 109244
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-117A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1722A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1722A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.7A>G
  hgvsp: ENSP00000362270.4:p.Lys3Glu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.7A>G
  hgvsp: ENSP00000362282.4:p.Lys3Glu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.7A>G
  hgvsp: ENSP00000410809.2:p.Lys3Glu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-117A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-117A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.7A>G
  hgvsp: ENSP00000416478.2:p.Lys3Glu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-117A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-117A>G
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys3Glu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-39895312-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895312
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895312
    reference: chr 6
allele count: 11
allele frequency: 1.006975594573317e-4
allele num: 109238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1723G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-118G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.6G>T
  hgvsp: ENSP00000362282.4:p.Trp2Cys
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.6G>T
  hgvsp: ENSP00000416478.2:p.Trp2Cys
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-118G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.6G>T
  hgvsp: ENSP00000362270.4:p.Trp2Cys
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.6G>T
  hgvsp: ENSP00000410809.2:p.Trp2Cys
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-118G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1723G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-118G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-118G>T
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31123
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11213
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp2Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-39895315-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895315
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895316
    reference: chr 6
allele count: 2
allele frequency: 1.83073064460026e-5
allele num: 109246
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-122_-138-121insA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-122_124-121insA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1727_-11-1726insA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.2_3insA
  hgvsp: ENSP00000362282.4:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-122_124-121insA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-122_124-121insA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.2_3insA
  hgvsp: ENSP00000410809.2:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1727_131-1726insA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.2_3insA
  hgvsp: ENSP00000362270.4:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.2_3insA
  hgvsp: ENSP00000416478.2:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-122_124-121insA
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

6-39895315-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895315
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895313
    reference: chr 6
allele count: 2
allele frequency: 1.83073064460026e-5
allele num: 109246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-123_124-122delAT
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.1_2delAT
  hgvsp: ENSP00000362270.4:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.1_2delAT
  hgvsp: ENSP00000410809.2:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-123_124-122delAT
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.1_2delAT
  hgvsp: ENSP00000362282.4:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.1_2delAT
  hgvsp: ENSP00000416478.2:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-123_124-122delAT
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-123_-138-122delAT
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-123_124-122delAT
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1728_131-1727delAT
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1728_-11-1727delAT
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30830
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
reference allele: CAT
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

6-39895316-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895316
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895316
    reference: chr 6
allele count: 1
allele frequency: 9.1471223153196e-6
allele num: 109324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.2T>C
  hgvsp: ENSP00000416478.2:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  hgvsc: ENST00000373175.4:c.2T>C
  hgvsp: ENSP00000362270.4:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.2T>C
  hgvsp: ENSP00000362282.4:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-122T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-122T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-122T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  hgvsc: ENST00000432280.2:c.2T>C
  hgvsp: ENSP00000410809.2:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1727T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-122T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1727T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-122T>C
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6499
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

6-39895316-ATG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895316
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895314
    reference: chr 6
allele count: 22
allele frequency: 2.012366909370312e-4
allele num: 109324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-124_-138-123delCA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000410809
  ensembl transcript: ENST00000432280
  gene symbol: MOCS1
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-1_1delCA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-124_124-123delCA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-124_124-123delCA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-124_124-123delCA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1729_-11-1728delCA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-124_124-123delCA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1729_131-1728delCA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.-1_1delCA
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362270
  ensembl transcript: ENST00000373175
  gene symbol: MOCS1
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: coding sequence
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6499
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11229
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30980
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: ATG
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

6-39895325-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895325
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895325
    reference: chr 6
allele count: 1
allele frequency: 9.160529112161519e-6
allele num: 109164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1736G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-131G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-131G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000416478
  ensembl transcript: ENST00000425303
  gene symbol: MOCS1
  hgvsc: ENST00000425303.2:c.-8G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-8G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-131G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-131G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1736G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-131G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6964
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8391
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1422
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

6-39895331-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895331
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895331
    reference: chr 6
allele count: 5
allele frequency: 4.581187810375474e-5
allele num: 109142
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-137T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1742T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-14T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1742T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-137T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-137T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-137T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-137T>C
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1402
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8464
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1427
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

6-39895332-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895332
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895332
    reference: chr 6
allele count: 1
allele frequency: 9.161871953677575e-6
allele num: 109148
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-15T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-138T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-138T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-138T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-138T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1743T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1743T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-138T>C
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28628
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2579
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1388
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-39895334-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895334
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895334
    reference: chr 6
allele count: 1
allele frequency: 9.165230780511052e-6
allele num: 109108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1745C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-140C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1745C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-140C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-17C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-140C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-140C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-140C>T
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11339
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4365
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33423
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ

6-39895338-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895338
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895338
    reference: chr 6
allele count: 2
allele frequency: 1.835940368656826e-5
allele num: 108936
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-144C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-21C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1749C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-144C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1749C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-144C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-144C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-144C>G
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8155
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27492
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3889
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1789
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1420
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD

6-39895339-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895339
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895339
    reference: chr 6
allele count: 1
allele frequency: 9.178353770467728e-6
allele num: 108952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-145C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-145C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1750C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-22C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-145C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-145C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1750C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-145C>T
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8153
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8548
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32010
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-39895352-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895352
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895352
    reference: chr 6
allele count: 1
allele frequency: 9.211326246753007e-6
allele num: 108562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1763C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1763C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-158C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-158C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-158C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-158C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-158C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-35C>T
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8039
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23377
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

6-39895352-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895352
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895352
    reference: chr 6
allele count: 1
allele frequency: 9.211326246753007e-6
allele num: 108562
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1763C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-158C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-35C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-158C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-158C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-158C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-158C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1763C>G
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8039
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1392
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27689
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

6-39895357-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895357
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895357
    reference: chr 6
allele count: 1
allele frequency: 9.23599822668834e-6
allele num: 108272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-163A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-163A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-163A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-40A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1768A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-163A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-163A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1768A>G
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9559
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26081
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1333
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2839
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

6-39895358-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895358
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895358
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 108214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-164G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-41G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1769G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-164G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-164G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-164G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1769G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-164G>C
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9833
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5281
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10003
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2083
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1754
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25588
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1392
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8186
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

6-39895360-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895360
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895360
    reference: chr 6
allele count: 1
allele frequency: 9.266466510990029e-6
allele num: 107916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1771G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-166G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1771G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-166G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-166G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-166G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-166G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-43G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10067
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21831
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8072
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2465
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2868
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4201
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1376
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

6-39895361-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895361
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895361
    reference: chr 6
allele count: 57
allele frequency: 5.290219590518442e-4
allele num: 107746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-167C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-167C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-44C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-167C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-167C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1772C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-167C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1772C>T
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21956
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8723
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 9655
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5379
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10052
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1187
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4409
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1009
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 9.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

6-39895364-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895364
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895364
    reference: chr 6
allele count: 5
allele frequency: 4.64701290010781e-5
allele num: 107596
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-170C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-170C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-47C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1775C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1775C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-170C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-170C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-170C>T
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10012
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9315
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2874
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1388
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4509
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4485
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

6-39895366-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895366
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895366
    reference: chr 6
allele count: 2
allele frequency: 1.860049849335962e-5
allele num: 107524
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-49C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-172C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-172C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-172C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-172C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-172C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1777C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1777C>T
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9995
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2882
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3796
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1397
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4543
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-39895369-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39895369
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39895369
    reference: chr 6
allele count: 1
allele frequency: 9.344571738277235e-6
allele num: 107014
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-11-1780T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362282
  ensembl transcript: ENST00000373186
  gene symbol: MOCS1
  hgvsc: ENST00000373186.4:c.-52T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.124-175T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.124-175T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.131-1780T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.124-175T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.124-175T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362277
  ensembl transcript: ENST00000373181
  gene symbol: MOCS1
  hgvsc: ENST00000373181.4:c.-138-175T>C
  variant of: http://identifiers.org/hgnc/7190
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9988
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8689
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6420
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3724
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2099
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2426
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

6-39901983-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39901983
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39901983
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 12656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+51G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+51G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+51G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+51G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+51G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+51G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25741
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4831
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1644
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1756
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17941
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16008
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3327
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8776
  bin: 1.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-39901986-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39901986
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39901986
    reference: chr 6
allele count: 1
allele frequency: 7.896399241945672e-5
allele num: 12664
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+48C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+48C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+48C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+48C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+48C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+48C>T
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23441
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2611
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17837
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4789
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18615
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ

6-39901987-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39901987
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39901987
    reference: chr 6
allele count: 1
allele frequency: 7.954183900731785e-5
allele num: 12572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+47C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+47C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+47C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+47C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+47C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+47C>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23430
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5486
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2709
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1740
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17732
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18607
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ

6-39901993-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39901993
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39901993
    reference: chr 6
allele count: 28
allele frequency: 2.233923727461305e-3
allele num: 12534
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+41G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+41G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+41G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+41G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+41G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+41G>C
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 1.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26095
  bin: 7.5e0
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23056
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1686
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4407
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  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4161
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 9.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 1516
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genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.25e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

6-39901994-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39901994
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39901994
    reference: chr 6
allele count: 3
allele frequency: 2.380574511982225e-4
allele num: 12602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+40G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+40G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+40G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+40G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+40G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+40G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23030
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4289
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4067
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1517
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21422
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1693
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

6-39901995-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39901995
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39901995
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 12656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+39A>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+39A>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+39A>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+39A>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+39A>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+39A>T
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 22971
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26248
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1682
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4131
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1782
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21742
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19540
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

6-39901999-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39901999
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39901999
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 12732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+35G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+35G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+35G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+35G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+35G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+35G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22532
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3260
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23308
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3382
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19828
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
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: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

6-39902000-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902000
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902000
    reference: chr 6
allele count: 1
allele frequency: 7.896399241945672e-5
allele num: 12664
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+34G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+34G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+34G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+34G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+34G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+34G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22339
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26817
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2976
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1637
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23698
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1692
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-39902009-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902009
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902009
    reference: chr 6
allele count: 1
allele frequency: 7.618467164406521e-5
allele num: 13126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+25C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+25C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+25C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+25C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+25C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+25C>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27424
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21677
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1373
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1113
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2443
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2451
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20334
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25199
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

6-39902013-A-ACG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902013
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902015
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 13208
alternate allele: ACG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+19_123+20dupCG
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+19_123+20dupCG
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+19_130+20dupCG
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+19_-12+20dupCG
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+19_123+20dupCG
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+19_123+20dupCG
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21788
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27186
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2551
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1138
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20602
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

6-39902016-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902016
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902016
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 13086
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+18G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+18G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+18G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+18G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+18G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+18G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26425
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2854
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22590
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20989
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1566
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
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genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

6-39902020-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902020
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902020
    reference: chr 6
allele count: 47
allele frequency: 3.724837533682042e-3
allele num: 12618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+14G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+14G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+14G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+14G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+14G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+14G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22418
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 1.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 57
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4221
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 21245
  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 534
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genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 2.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 21041
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 44
  bin: 9.75e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 7
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  variant carriers: 6
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

6-39902021-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902021
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902021
    reference: chr 6
allele count: 1
allele frequency: 7.611508601004719e-5
allele num: 13138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+13C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+13C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+13C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+13C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+13C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+13C>T
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
  all individuals: 409
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 654
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 69
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genotype quality: GenotypeQuality
  all individuals: 3001
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD

6-39902022-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902022
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902022
    reference: chr 6
allele count: 7
allele frequency: 5.265533323303746e-4
allele num: 13294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+12C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+12C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+12C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+12C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+12C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+12C>T
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25910
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22448
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21529
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21952
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-39902025-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902025
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902025
    reference: chr 6
allele count: 66
allele frequency: 8.264462809917356e-3
allele num: 7986
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-12+9A>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.130+9A>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.123+9A>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.123+9A>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.123+9A>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.123+9A>C
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: intron
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 1.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22903
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25797
  bin: 7.5e0
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 3.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 2.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3583
  bin: 1.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 20526
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5089
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 8055
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 15404
  bin: 2.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 6.25e1
  variant carriers: 4
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

6-39902038-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902038
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902038
    reference: chr 6
allele count: 3
allele frequency: 2.550153009180551e-4
allele num: 11764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.119C>T
  hgvsp: ENSP00000344794.5:p.Ser40Leu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.119C>T
  hgvsp: ENSP00000309843.7:p.Ser40Leu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-16C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.119C>T
  hgvsp: ENSP00000362284.2:p.Ser40Leu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.119C>T
  hgvsp: ENSP00000418315.1:p.Ser40Leu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.126C>T
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23749
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25029
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3638
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18587
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1841
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser40Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

6-39902041-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902041
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902041
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 11898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-19C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.123C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.116C>T
  hgvsp: ENSP00000344794.5:p.Ala39Val
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.116C>T
  hgvsp: ENSP00000362284.2:p.Ala39Val
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.116C>T
  hgvsp: ENSP00000418315.1:p.Ala39Val
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.116C>T
  hgvsp: ENSP00000309843.7:p.Ala39Val
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23511
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23784
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1771
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3632
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala39Val
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

6-39902045-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902045
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902045
    reference: chr 6
allele count: 1
allele frequency: 8.259002312520647e-5
allele num: 12108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.112G>C
  hgvsp: ENSP00000418315.1:p.Ala38Pro
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.112G>C
  hgvsp: ENSP00000362284.2:p.Ala38Pro
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-23G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.119G>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.112G>C
  hgvsp: ENSP00000344794.5:p.Ala38Pro
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.112G>C
  hgvsp: ENSP00000309843.7:p.Ala38Pro
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25434
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22932
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23868
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1934
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3938
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3338
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala38Pro
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-39902052-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902052
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902052
    reference: chr 6
allele count: 2
allele frequency: 1.533742331288344e-4
allele num: 13040
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.105C>T
  hgvsp: ENST00000487924.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-30C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.105C>T
  hgvsp: ENST00000373188.2:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.105C>T
  hgvsp: ENST00000340692.5:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.112C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.105C>T
  hgvsp: ENST00000308559.7:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25633
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24029
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2044
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3428
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3068
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Ser35Ser
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

6-39902055-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902055
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902055
    reference: chr 6
allele count: 1
allele frequency: 7.456009543692216e-5
allele num: 13412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.109G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.102G>A
  hgvsp: ENST00000487924.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.102G>A
  hgvsp: ENST00000340692.5:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.102G>A
  hgvsp: ENST00000373188.2:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.102G>A
  hgvsp: ENST00000308559.7:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-33G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25762
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24064
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1975
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3497
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu34Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

6-39902061-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902061
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902061
    reference: chr 6
allele count: 24
allele frequency: 1.706727350305789e-3
allele num: 14062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-39C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.96C>T
  hgvsp: ENST00000487924.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.96C>T
  hgvsp: ENST00000373188.2:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.103C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.96C>T
  hgvsp: ENST00000308559.7:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.96C>T
  hgvsp: ENST00000340692.5:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21605
  bin: 7.5e0
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 25716
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2961
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2107
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16367
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3289
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24098
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro32Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

6-39902061-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902061
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902061
    reference: chr 6
allele count: 1
allele frequency: 7.111363959607453e-5
allele num: 14062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.96C>G
  hgvsp: ENST00000373188.2:c.96C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.96C>G
  hgvsp: ENST00000340692.5:c.96C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-39C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.103C>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.96C>G
  hgvsp: ENST00000487924.1:c.96C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.96C>G
  hgvsp: ENST00000308559.7:c.96C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21605
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2107
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16367
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24098
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro32Pro
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

6-39902075-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902075
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902075
    reference: chr 6
allele count: 1
allele frequency: 6.871907641561298e-5
allele num: 14552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.82A>T
  hgvsp: ENSP00000362284.2:p.Thr28Ser
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-53A>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.82A>T
  hgvsp: ENSP00000418315.1:p.Thr28Ser
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.82A>T
  hgvsp: ENSP00000309843.7:p.Thr28Ser
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.82A>T
  hgvsp: ENSP00000344794.5:p.Thr28Ser
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.89A>T
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25665
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21736
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24052
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3166
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16250
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1888
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
hgvs: p.Thr28Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-39902080-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902080
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902080
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 14724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-58C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.84C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.77C>A
  hgvsp: ENSP00000418315.1:p.Pro26Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.77C>A
  hgvsp: ENSP00000309843.7:p.Pro26Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.77C>A
  hgvsp: ENSP00000344794.5:p.Pro26Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.77C>A
  hgvsp: ENSP00000362284.2:p.Pro26Gln
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25415
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22079
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3010
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23948
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1663
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4760
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2679
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro26Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-39902084-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902084
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902084
    reference: chr 6
allele count: 1
allele frequency: 6.745817593092283e-5
allele num: 14824
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.73G>T
  hgvsp: ENSP00000344794.5:p.Ala25Ser
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.73G>T
  hgvsp: ENSP00000362284.2:p.Ala25Ser
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.80G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-62G>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.73G>T
  hgvsp: ENSP00000309843.7:p.Ala25Ser
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.73G>T
  hgvsp: ENSP00000418315.1:p.Ala25Ser
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4798
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3007
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2931
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23789
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17296
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala25Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

6-39902096-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902096
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902096
    reference: chr 6
allele count: 2
allele frequency: 1.320306311064167e-4
allele num: 15148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.61T>C
  hgvsp: ENSP00000362284.2:p.Cys21Arg
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.61T>C
  hgvsp: ENSP00000418315.1:p.Cys21Arg
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.68T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.61T>C
  hgvsp: ENSP00000309843.7:p.Cys21Arg
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-74T>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.61T>C
  hgvsp: ENSP00000344794.5:p.Cys21Arg
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24529
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17372
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3063
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23126
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4849
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys21Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

6-39902101-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902101
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902101
    reference: chr 6
allele count: 1
allele frequency: 6.624271330153684e-5
allele num: 15096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.56G>A
  hgvsp: ENSP00000344794.5:p.Arg19Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.56G>A
  hgvsp: ENSP00000362284.2:p.Arg19Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.56G>A
  hgvsp: ENSP00000418315.1:p.Arg19Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.56G>A
  hgvsp: ENSP00000309843.7:p.Arg19Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-79G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.63G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23938
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18286
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3396
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4873
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg19Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

6-39902102-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902102
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902102
    reference: chr 6
allele count: 1
allele frequency: 6.597176408497163e-5
allele num: 15158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.55C>T
  hgvsp: ENSP00000344794.5:p.Arg19Trp
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.62C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-80C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.55C>T
  hgvsp: ENSP00000362284.2:p.Arg19Trp
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.55C>T
  hgvsp: ENSP00000309843.7:p.Arg19Trp
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.55C>T
  hgvsp: ENSP00000418315.1:p.Arg19Trp
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23700
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19091
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2813
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2988
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1582
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4907
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genotype quality: GenotypeQuality
  all individuals: 22481
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg19Trp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

6-39902134-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902134
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902134
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 17046
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.23G>A
  hgvsp: ENSP00000309843.7:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.23G>A
  hgvsp: ENSP00000344794.5:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.30G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.23G>A
  hgvsp: ENSP00000418315.1:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.23G>A
  hgvsp: ENSP00000362284.2:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-112G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28872
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18626
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17939
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25367
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1913
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg8Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

6-39902146-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902146
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902146
    reference: chr 6
allele count: 2
allele frequency: 1.122334455667789e-4
allele num: 17820
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.11G>A
  hgvsp: ENSP00000309843.7:p.Arg4Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.11G>A
  hgvsp: ENSP00000362284.2:p.Arg4Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.11G>A
  hgvsp: ENSP00000344794.5:p.Arg4Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.11G>A
  hgvsp: ENSP00000418315.1:p.Arg4Gln
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.18G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-124G>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29831
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2754
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5393
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1595
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26831
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg4Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

6-39902147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902147
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902147
    reference: chr 6
allele count: 1
allele frequency: 5.630630630630631e-5
allele num: 17760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.10C>T
  hgvsp: ENSP00000418315.1:p.Arg4Trp
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.10C>T
  hgvsp: ENSP00000344794.5:p.Arg4Trp
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.10C>T
  hgvsp: ENSP00000362284.2:p.Arg4Trp
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-125C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.17C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.10C>T
  hgvsp: ENSP00000309843.7:p.Arg4Trp
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5349
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26458
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3074
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16655
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg4Trp
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

6-39902152-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902152
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902152
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 18248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.5C>T
  hgvsp: ENSP00000309843.7:p.Ala2Val
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.5C>T
  hgvsp: ENSP00000362284.2:p.Ala2Val
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.5C>T
  hgvsp: ENSP00000344794.5:p.Ala2Val
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.5C>T
  hgvsp: ENSP00000418315.1:p.Ala2Val
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-130C>T
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.12C>T
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16844
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30446
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16418
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28228
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2448
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala2Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum

6-39902152-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902152
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902152
    reference: chr 6
allele count: 1
allele frequency: 5.480052608505042e-5
allele num: 18248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.5C>A
  hgvsp: ENSP00000344794.5:p.Ala2Glu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.5C>A
  hgvsp: ENSP00000309843.7:p.Ala2Glu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.5C>A
  hgvsp: ENSP00000418315.1:p.Ala2Glu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.5C>A
  hgvsp: ENSP00000362284.2:p.Ala2Glu
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-130C>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.12C>A
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16844
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5487
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2448
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16418
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala2Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS

6-39902153-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902153
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902153
    reference: chr 6
allele count: 3
allele frequency: 1.623552332503518e-4
allele num: 18478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.4G>A
  hgvsp: ENSP00000362284.2:p.Ala2Thr
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.11G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-131G>A
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.4G>A
  hgvsp: ENSP00000344794.5:p.Ala2Thr
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.4G>A
  hgvsp: ENSP00000418315.1:p.Ala2Thr
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.4G>A
  hgvsp: ENSP00000309843.7:p.Ala2Thr
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16733
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30650
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2085
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 1
hgvs: p.Ala2Thr
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

6-39902156-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902156
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902156
    reference: chr 6
allele count: 11
allele frequency: 5.889281507656066e-4
allele num: 18678
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124615
  ensembl transcript: ENST00000473742
  gene symbol: MOCS1
  hgvsc: ENST00000473742.1:n.8A>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.1A>C
  hgvsp: ENSP00000362284.2:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.1A>C
  hgvsp: ENSP00000418315.1:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.1A>C
  hgvsp: ENSP00000309843.7:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-134A>C
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000344794
  ensembl transcript: ENST00000340692
  gene symbol: MOCS1
  hgvsc: ENST00000340692.5:c.1A>C
  hgvsp: ENSP00000344794.5:p.Met1?
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16730
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30612
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2175
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28928
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16405
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

6-39902166-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 39902166
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 39902166
    reference: chr 6
allele count: 1
allele frequency: 5.277601857715854e-5
allele num: 18948
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362284
  ensembl transcript: ENST00000373188
  gene symbol: MOCS1
  hgvsc: ENST00000373188.2:c.-10A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000309843
  ensembl transcript: ENST00000308559
  gene symbol: MOCS1
  hgvsc: ENST00000308559.7:c.-10A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000418315
  ensembl transcript: ENST00000487924
  gene symbol: MOCS1
  hgvsc: ENST00000487924.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/7190
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000124615
  ensembl protein: ENSP00000362291
  ensembl transcript: ENST00000373195
  gene symbol: MOCS1
  hgvsc: ENST00000373195.3:c.-144A>G
  variant of: http://identifiers.org/hgnc/7190
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17311
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29861
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17024
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2003
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28633
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 736
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1281
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 199
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1259
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3362
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26636
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3730
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 417
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10954
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 9.75e1
variant carriers: 262

GenotypeQuality
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2357
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1255
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3662
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 697
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 667
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1184
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 977
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 238
bin: 8.75e1
variant carriers: 1

Latino
type: Population
allele count: 5
allele frequency: 4.855311711011847e-4
allele num: 10298
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.694760820045558e-4
allele num: 8780
num of homozygotes: 0

South Asian
type: Population
allele count: 18
allele frequency: 1.209352324643913e-3
allele num: 14884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 20
allele frequency: 3.608805485384338e-3
allele num: 5542
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 224
allele frequency: 3.892402863696393e-3
allele num: 57548
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 6.493506493506494e-3
allele num: 770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7944
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.38e-1

DP
type: SiteQuality
SIO_000300: 1.171392e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.314e1

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.98e0

GenotypeQuality
all individuals: 417
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26636
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3362
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 238
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3730
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10954
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1281
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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bin: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7944
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.737679849864461e-5
allele num: 57548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14884
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8780
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

FS
type: SiteQuality
SIO_000300: 5.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
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SIO_000300: 3.98e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e-1

DP
type: SiteQuality
SIO_000300: 1.171392e6

QD
type: SiteQuality
SIO_000300: 1.314e1

GenotypeQuality
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bin: 1.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.255965837729214e-4
allele num: 7962
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8778
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.471619510501649e-5
allele num: 57610
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5530
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 14868
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

MQRankSum
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SIO_000300: 0.0e0

DP
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InbreedingCoeff
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 2.0938e1

MQ
type: SiteQuality
SIO_000300: 5.866e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.52e-1

QD
type: SiteQuality
SIO_000300: 1.034e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.15e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8778
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5530
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.0938e1

VQSLOD
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MQ
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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SIO_000300: 3.52e-1

QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.17791e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8836
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8058
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.722949689869056e-5
allele num: 58040
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14924
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

DP
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SIO_000300: 1.193256e6

InbreedingCoeff
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SIO_000300: -2.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.881e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-1

QD
type: SiteQuality
SIO_000300: 1.008e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8846
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.722890320802178e-5
allele num: 58042
num of homozygotes: 0

East Asian
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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: 14920
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

FS
type: SiteQuality
SIO_000300: 1.1277e1

QD
type: SiteQuality
SIO_000300: 1.089e1

ClippingRankSum
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SIO_000300: 2.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.218e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.73e-1

MQ
type: SiteQuality
SIO_000300: 5.866e1

DP
type: SiteQuality
SIO_000300: 1.19699e6

BaseQRankSum
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SIO_000300: -1.268e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.24e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8874
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.710278775440397e-5
allele num: 58470
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.206941e6

FS
type: SiteQuality
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ReadPosRankSum
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QD
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VQSLOD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 1.42e-1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10488
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.687174000267486e-5
allele num: 14954
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ClippingRankSum
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ReadPosRankSum
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DP
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MQ
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FS
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.105340185834383e-5
allele num: 58762
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14958
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: -8.763e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

QD
type: SiteQuality
SIO_000300: 1.101e1

FS
type: SiteQuality
SIO_000300: 9.755000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 1.222824e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
all individuals: 780
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1403
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14972
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5684
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.361721201255042e-4
allele num: 8924
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58872
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.923e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.03e-1

DP
type: SiteQuality
SIO_000300: 1.229106e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-1

QD
type: SiteQuality
SIO_000300: 1.518e1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.156e0

GenotypeQuality
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bin: 2.25e1
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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 425
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variant carriers: 8

GenotypeQuality
all individuals: 2107
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.351168760978246e-4
allele num: 59208
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8992
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10576
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

DP
type: SiteQuality
SIO_000300: 1.2498e6

QD
type: SiteQuality
SIO_000300: 1.162e1

MQRankSum
type: SiteQuality
SIO_000300: 5.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.244e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

GenotypeQuality
all individuals: 1430
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 805
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 649
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variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15020
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.68662506324844e-5
allele num: 59290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8992
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8274
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.419999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.015e1

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.54e-1

FS
type: SiteQuality
SIO_000300: 1.959e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

QD
type: SiteQuality
SIO_000300: 1.474e1

DP
type: SiteQuality
SIO_000300: 1.251435e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.162e0

GenotypeQuality
all individuals: 513
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variant carriers: 0

GenotypeQuality
all individuals: 595
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GenotypeQuality
all individuals: 4401
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GenotypeQuality
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GenotypeQuality
all individuals: 2016
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 69
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 474
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 824
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GenotypeQuality
all individuals: 1990
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.887861053426468e-4
allele num: 10594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15030
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.754e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

QD
type: SiteQuality
SIO_000300: 7.71e0

FS
type: SiteQuality
SIO_000300: 6.192e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.64e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.05e-1

DP
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SIO_000300: 1.258041e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.89e-1

GenotypeQuality
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variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9006
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.666666666666667e-5
allele num: 15000
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59284
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 1.757e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

BaseQRankSum
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SIO_000300: 1.51e0

DP
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SIO_000300: 1.260544e6

VQSLOD
type: SiteQuality
SIO_000300: 3.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e-1

QD
type: SiteQuality
SIO_000300: 1.629e1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9064
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10666
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15050
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.678640972268851e-5
allele num: 59572
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.45e0

FS
type: SiteQuality
SIO_000300: 3.319e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.88e-1

DP
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InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 11

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

GenotypeQuality
all individuals: 221
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5782
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.212789415656009e-3
allele num: 9070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15050
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10662
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5794
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15066
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9058
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10670
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.358635050715389e-5
allele num: 59548
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

QD
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SIO_000300: 1.437e1

MQ
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SIO_000300: 6.051e1

VQSLOD
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BaseQRankSum
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SIO_000300: 2.44e-1

FS
type: SiteQuality
SIO_000300: 7.777e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

DP
type: SiteQuality
SIO_000300: 1.268861e6

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.679317525357695e-5
allele num: 59548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5794
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10670
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15066
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.103996467211305e-4
allele num: 9058
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.777e0

BaseQRankSum
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InbreedingCoeff
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SIO_000300: 2.8e-3

MQRankSum
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

DP
type: SiteQuality
SIO_000300: 1.268861e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.051e1

QD
type: SiteQuality
SIO_000300: 1.437e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9068
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.638343069569835e-5
allele num: 15064
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59598
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5796
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.26972e6

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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ReadPosRankSum
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SIO_000300: 4.72e-1

InbreedingCoeff
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SIO_000300: 2.6e-3

FS
type: SiteQuality
SIO_000300: 5.25e-1

QD
type: SiteQuality
SIO_000300: 1.58e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15064
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59598
num of homozygotes: 0

Latino
type: Population
allele count: 22
allele frequency: 2.059925093632959e-3
allele num: 10680
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.06e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.26972e6

MQRankSum
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SIO_000300: 6.26e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

FS
type: SiteQuality
SIO_000300: 5.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.63e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.681463545870325e-5
allele num: 59472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9050
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15070
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5792
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.385e0

DP
type: SiteQuality
SIO_000300: 1.26283e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

BaseQRankSum
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SIO_000300: -4.728e0

QD
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VQSLOD
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

East Asian
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allele count: 5
allele frequency: 6.031363088057901e-4
allele num: 8290
num of homozygotes: 0

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

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

South Asian
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African
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allele frequency: 0.0e0
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Latino
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QD
type: SiteQuality
SIO_000300: 1.006e1

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.096e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.251839e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5800
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.682651859330305e-5
allele num: 59430
num of homozygotes: 0

Latino
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South Asian
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African
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Other
type: Population
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num of homozygotes: 0

East Asian
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BaseQRankSum
type: SiteQuality
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DP
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FS
type: SiteQuality
SIO_000300: 1.9393e1

MQRankSum
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ClippingRankSum
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VQSLOD
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QD
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SIO_000300: 1.143e1

MQ
type: SiteQuality
SIO_000300: 5.915e1

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.24e-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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African
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allele count: 0
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European (Non-Finnish)
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European (Finnish)
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Latino
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East Asian
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Other
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South Asian
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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FS
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QD
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4260
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5778
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10692
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9054
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.328550551348479e-4
allele num: 15054
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 1.242565e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

VQSLOD
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SIO_000300: 1.7e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.98e-1

QD
type: SiteQuality
SIO_000300: 1.191e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59296
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.104972375690608e-4
allele num: 9050
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5774
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15054
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

DP
type: SiteQuality
SIO_000300: 1.242342e6

VQSLOD
type: SiteQuality
SIO_000300: 2.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.093e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10698
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.695720002713152e-5
allele num: 58972
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5746
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8274
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9030
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

FS
type: SiteQuality
SIO_000300: 9.92e-1

QD
type: SiteQuality
SIO_000300: 1.164e1

VQSLOD
type: SiteQuality
SIO_000300: 6.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.63e-1

DP
type: SiteQuality
SIO_000300: 1.207996e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.107419712070875e-4
allele num: 9030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10698
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15048
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58972
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8274
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

FS
type: SiteQuality
SIO_000300: 9.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

QD
type: SiteQuality
SIO_000300: 1.164e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

DP
type: SiteQuality
SIO_000300: 1.207996e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 1885
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variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.701664227614607e-5
allele num: 58766
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10672
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.05e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.496e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.11e-1

DP
type: SiteQuality
SIO_000300: 1.197425e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-1

QD
type: SiteQuality
SIO_000300: 7.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8252
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15030
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10680
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.179e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -8.133e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-2

DP
type: SiteQuality
SIO_000300: 1.195291e6

QD
type: SiteQuality
SIO_000300: 1.662e1

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: 3859
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5712
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15014
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8996
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.21300339640951e-4
allele num: 8244
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.402e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

FS
type: SiteQuality
SIO_000300: 1.0366e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 1.191486e6

VQSLOD
type: SiteQuality
SIO_000300: -2.467e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 55

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.198753296571566e-4
allele num: 58394
num of homozygotes: 0

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

East Asian
type: Population
allele count: 39
allele frequency: 4.729565850109143e-3
allele num: 8246
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.11632060727841e-3
allele num: 8958
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.272264631043257e-3
allele num: 786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10640
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5716
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

QD
type: SiteQuality
SIO_000300: 1.221e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 785
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.864831468387451e-5
allele num: 58268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8230
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.389671361502347e-5
allele num: 10650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15010
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8960
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5698
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.413e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 1.186677e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.38e-1

QD
type: SiteQuality
SIO_000300: 1.037e1

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
all individuals: 4548
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2409
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.431315341599805e-4
allele num: 8226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58220
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15000
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8958
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5696
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10640
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.187051e6

QD
type: SiteQuality
SIO_000300: 6.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

FS
type: SiteQuality
SIO_000300: 1.7094e1

VQSLOD
type: SiteQuality
SIO_000300: -2.466e0

MQRankSum
type: SiteQuality
SIO_000300: 8.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e-1

GenotypeQuality
all individuals: 1104
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16411
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8916
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.680919294494922e-5
allele num: 14968
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57838
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5674
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.693e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.76e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

DP
type: SiteQuality
SIO_000300: 1.192125e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

QD
type: SiteQuality
SIO_000300: 1.517e1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 3
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1222
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 946
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 926
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.19548e5

QD
type: SiteQuality
SIO_000300: 1.39e1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1603
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 944
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7586
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1210
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.091703056768559e-3
allele num: 916
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1616
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.262e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.21174e5

VQSLOD
type: SiteQuality
SIO_000300: -6.36e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.48e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

QD
type: SiteQuality
SIO_000300: 1.537e1

MQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.829e1

GenotypeQuality
all individuals: 4768
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
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variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7522
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 8.183306055646482e-4
allele num: 1222
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.95e0

VQSLOD
type: SiteQuality
SIO_000300: -1.815e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 3.21157e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 2.808e0

QD
type: SiteQuality
SIO_000300: 8.199999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 19369
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 3
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2098
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 178
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 6
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 21041
bin: 2.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1194
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.143200962695548e-2
allele num: 1662
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 916
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.202565473009086e-3
allele num: 7484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

FS
type: SiteQuality
SIO_000300: 2.802e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.26e-2

DP
type: SiteQuality
SIO_000300: 3.28196e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.393e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1920
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variant carriers: 0

GenotypeQuality
all individuals: 19467
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GenotypeQuality
all individuals: 322
bin: 6.25e1
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GenotypeQuality
all individuals: 162
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 2

GenotypeQuality
all individuals: 18
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variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.247191011235955e-3
allele num: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.334044823906083e-4
allele num: 7496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 922
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1688
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 8.779999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.43e-2

DP
type: SiteQuality
SIO_000300: 3.28854e5

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 17
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GenotypeQuality
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 0
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 920
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1712
num of homozygotes: 0

African
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: 1238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7510
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.616e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.37e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 3.2963e5

VQSLOD
type: SiteQuality
SIO_000300: -5.876e-1

QD
type: SiteQuality
SIO_000300: 8.6e0

GenotypeQuality
all individuals: 509
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1234
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7528
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 910
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.377e0

DP
type: SiteQuality
SIO_000300: 3.35133e5

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

FS
type: SiteQuality
SIO_000300: 1.464e0

QD
type: SiteQuality
SIO_000300: 9.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.36e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1226
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.334757074212493e-4
allele num: 7492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1790
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.3728e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.221e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

InbreedingCoeff
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SIO_000300: -4.41e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.627e1

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
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GenotypeQuality
all individuals: 409
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variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1634
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1222
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.079913606911447e-3
allele num: 926
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2116
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

DP
type: SiteQuality
SIO_000300: 3.44759e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.32e-2

MQ
type: SiteQuality
SIO_000300: 5.395e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.31e0

VQSLOD
type: SiteQuality
SIO_000300: -7.485000000000001e-1

GenotypeQuality
all individuals: 8
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24721
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1594
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2541
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7608
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.41e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.49e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

DP
type: SiteQuality
SIO_000300: 3.4407e5

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.153e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

QD
type: SiteQuality
SIO_000300: 6.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 3573
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1194
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

DP
type: SiteQuality
SIO_000300: 3.40747e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 7.068e0

QD
type: SiteQuality
SIO_000300: 7.88e0

VQSLOD
type: SiteQuality
SIO_000300: -1.433e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.58e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1237
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 412
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 7
bin: 8.75e1
variant carriers: 7

GenotypeQuality
all individuals: 10
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variant carriers: 1

GenotypeQuality
all individuals: 53
bin: 6.75e1
variant carriers: 5

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1158
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 1.773049645390071e-2
allele num: 282
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2530
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 42
allele frequency: 6.065857885615251e-3
allele num: 6924
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 90
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.61e-2

DP
type: SiteQuality
SIO_000300: 3.41253e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.57e-1

QD
type: SiteQuality
SIO_000300: 1.04e1

FS
type: SiteQuality
SIO_000300: 1.757e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

GenotypeQuality
all individuals: 21431
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 8.605851979345956e-4
allele num: 1162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2750
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.65e-2

DP
type: SiteQuality
SIO_000300: 3.43029e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

FS
type: SiteQuality
SIO_000300: 1.706e0

VQSLOD
type: SiteQuality
SIO_000300: -4.55e-1

MQ
type: SiteQuality
SIO_000300: 5.843e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.01e0

GenotypeQuality
all individuals: 3537
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2986
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 72
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1150
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.250825082508251e-4
allele num: 7272
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 3.538570417551309e-4
allele num: 2826
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

FS
type: SiteQuality
SIO_000300: 2.604e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 3.42988e5

QD
type: SiteQuality
SIO_000300: 7.26e0

VQSLOD
type: SiteQuality
SIO_000300: -5.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.61e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

GenotypeQuality
all individuals: 1
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 7.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 138
bin: 4.75e1
variant carriers: 12

GenotypeQuality
all individuals: 104
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 7
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 276
bin: 3.75e1
variant carriers: 8

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

European (Finnish)
type: Population
allele count: 4
allele frequency: 2.898550724637681e-2
allele num: 138
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.41643059490085e-3
allele num: 706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 59
allele frequency: 1.65266106442577e-2
allele num: 3570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 8.006405124099279e-4
allele num: 2498
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.496e2

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.422e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.27e-2

QD
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 3.27525e5

FS
type: SiteQuality
SIO_000300: 2.34201e2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 16
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3197
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 23580
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 330
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.114961271911944e-4
allele num: 4906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.17e-1

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -9.49e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 3.30882e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-2

FS
type: SiteQuality
SIO_000300: 1.218e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.18e-2

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

GenotypeQuality
all individuals: 3257
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18257
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.17e-2

DP
type: SiteQuality
SIO_000300: 3.31798e5

QD
type: SiteQuality
SIO_000300: 5.41e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.635e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17090
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 5.25e1
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GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 106
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.107925801011804e-4
allele num: 4744
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.34709e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.15e0

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-1

QD
type: SiteQuality
SIO_000300: 1.377e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.29e-2

GenotypeQuality
all individuals: 725
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16295
bin: 2.25e1
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GenotypeQuality
all individuals: 61
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GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 80
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3613
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4876
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.277613897082924e-4
allele num: 6102
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.941e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.487e-1

DP
type: SiteQuality
SIO_000300: 3.45045e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.38e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 15882
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3725
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3239
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4988
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.570845114671693e-4
allele num: 6366
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.47741e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.39e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.115e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

MQRankSum
type: SiteQuality
SIO_000300: -2.11e-1

QD
type: SiteQuality
SIO_000300: 1.574e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

GenotypeQuality
all individuals: 17
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 3879
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 403
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 6
bin: 8.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 5

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

South Asian
type: Population
allele count: 8
allele frequency: 1.151410477835348e-3
allele num: 6948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 3.138485680659082e-3
allele num: 5098
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.307e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.48e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.91e0

DP
type: SiteQuality
SIO_000300: 3.57984e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 76
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3879
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2961
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 337
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3289
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.961553550411926e-4
allele num: 5098
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6948
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.48e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.307e1

VQSLOD
type: SiteQuality
SIO_000300: 4.91e0

DP
type: SiteQuality
SIO_000300: 3.57984e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3224
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 360
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4613
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.136752136752137e-3
allele num: 468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5118
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.68314e5

QD
type: SiteQuality
SIO_000300: 9.380000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 5.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.35e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

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

GenotypeQuality
all individuals: 88
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 17394
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 472
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.22e-2

FS
type: SiteQuality
SIO_000300: 1.822e0

QD
type: SiteQuality
SIO_000300: 1.444e1

VQSLOD
type: SiteQuality
SIO_000300: -8.394e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 3.7365e5

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 425
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 322
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.302083333333333e-4
allele num: 7680
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.389999999999999e-1

DP
type: SiteQuality
SIO_000300: 3.75638e5

MQ
type: SiteQuality
SIO_000300: 5.896e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.22e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.831e0

MQRankSum
type: SiteQuality
SIO_000300: 6.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
SIO_000300: -1.084e0

QD
type: SiteQuality
SIO_000300: 9.699999999999999e0

GenotypeQuality
all individuals: 53
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1595
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3610
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7722
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.672240802675585e-3
allele num: 598
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.049180327868853e-3
allele num: 488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-2

DP
type: SiteQuality
SIO_000300: 3.81139e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 4.304e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

QD
type: SiteQuality
SIO_000300: 9.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

VQSLOD
type: SiteQuality
SIO_000300: -1.117e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 22563
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.572327044025157e-3
allele num: 636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.95e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.98e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.925999999999999e-1

DP
type: SiteQuality
SIO_000300: 3.85634e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-1

GenotypeQuality
all individuals: 91
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.295001295001295e-4
allele num: 7722
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.571e-1

FS
type: SiteQuality
SIO_000300: 1.336e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.91e-2

QD
type: SiteQuality
SIO_000300: 1.375e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.28e-1

DP
type: SiteQuality
SIO_000300: 3.88452e5

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
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GenotypeQuality
all individuals: 2707
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5246
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7862
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 5.763e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.966e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.98e-2

QD
type: SiteQuality
SIO_000300: 8.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

DP
type: SiteQuality
SIO_000300: 4.28664e5

GenotypeQuality
all individuals: 428
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16651
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 198
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 459
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 1.184834123222749e-3
allele num: 844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.410437235543018e-4
allele num: 7090
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1006
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7906
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.73e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.87e-1

QD
type: SiteQuality
SIO_000300: 1.055e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.39011e5

GenotypeQuality
all individuals: 534
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.266143327424664e-4
allele num: 7898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1010
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7040
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.511e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.79e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.431e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.81e-2

DP
type: SiteQuality
SIO_000300: 4.39385e5

QD
type: SiteQuality
SIO_000300: 1.126e1

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5487
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 463
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7328
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1056
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 5.616e1

FS
type: SiteQuality
SIO_000300: 5.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.979e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.02e-2

QD
type: SiteQuality
SIO_000300: 8.75e0

DP
type: SiteQuality
SIO_000300: 4.48428e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 463
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28228
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.364628820960699e-4
allele num: 7328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7940
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1056
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

DP
type: SiteQuality
SIO_000300: 4.48428e5

QD
type: SiteQuality
SIO_000300: 8.75e0

MQ
type: SiteQuality
SIO_000300: 5.616e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.979e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.02e-2

FS
type: SiteQuality
SIO_000300: 5.62e0

GenotypeQuality
all individuals: 93
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16341
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 28949
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5571
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 3.325942350332594e-3
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7956
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.49832e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.752e0

VQSLOD
type: SiteQuality
SIO_000300: -4.129e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.55e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.92e0

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

GenotypeQuality
all individuals: 430
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 590
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5568
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7596
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 9.025270758122744e-4
allele num: 1108
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 932
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 1.255335174491589e-3
allele num: 7966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.052e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.49e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 4.51199e5