19-8509921-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509921
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509921
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 19122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.39G>A
  hgvsp: ENST00000600092.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.39G>A
  hgvsp: ENST00000600806.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.39G>A
  hgvsp: ENST00000325495.4:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.39G>A
  hgvsp: ENST00000594907.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.118G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.39G>A
  hgvsp: ENST00000601645.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.39G>A
  hgvsp: ENST00000348943.3:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.39G>A
  hgvsp: ENST00000596984.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33007
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15592
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2042
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala13Ala
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

19-8509923-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509923
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509923
    reference: chr 19
allele count: 1
allele frequency: 5.162089613875697e-5
allele num: 19372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.41C>T
  hgvsp: ENSP00000471339.1:p.Thr14Met
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.41C>T
  hgvsp: ENSP00000470932.1:p.Thr14Met
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.41C>T
  hgvsp: ENSP00000471530.1:p.Thr14Met
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.41C>T
  hgvsp: ENSP00000325376.2:p.Thr14Met
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.41C>T
  hgvsp: ENSP00000325732.2:p.Thr14Met
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.41C>T
  hgvsp: ENSP00000470017.1:p.Thr14Met
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.41C>T
  hgvsp: ENSP00000472789.1:p.Thr14Met
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.120C>T
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16004
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3815
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15428
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr14Met
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

19-8509924-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509924
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509924
    reference: chr 19
allele count: 1
allele frequency: 5.140859551717047e-5
allele num: 19452
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.42G>A
  hgvsp: ENST00000325495.4:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.42G>A
  hgvsp: ENST00000600092.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.42G>A
  hgvsp: ENST00000594907.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.42G>A
  hgvsp: ENST00000600806.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.121G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.42G>A
  hgvsp: ENST00000596984.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.42G>A
  hgvsp: ENST00000348943.3:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.42G>A
  hgvsp: ENST00000601645.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15899
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32756
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr14Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-8509926-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509926
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509926
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 19682
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.44A>C
  hgvsp: ENSP00000325376.2:p.Glu15Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.44A>C
  hgvsp: ENSP00000470017.1:p.Glu15Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.44A>C
  hgvsp: ENSP00000471339.1:p.Glu15Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.44A>C
  hgvsp: ENSP00000470932.1:p.Glu15Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.44A>C
  hgvsp: ENSP00000325732.2:p.Glu15Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.44A>C
  hgvsp: ENSP00000472789.1:p.Glu15Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.44A>C
  hgvsp: ENSP00000471530.1:p.Glu15Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.123A>C
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33218
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15913
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32735
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15417
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu15Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

19-8509927-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509927
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509927
    reference: chr 19
allele count: 1
allele frequency: 5.094243504839531e-5
allele num: 19630
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.45G>A
  hgvsp: ENST00000600806.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.45G>A
  hgvsp: ENST00000601645.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.45G>A
  hgvsp: ENST00000348943.3:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.45G>A
  hgvsp: ENST00000600092.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.45G>A
  hgvsp: ENST00000325495.4:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.124G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.45G>A
  hgvsp: ENST00000594907.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.45G>A
  hgvsp: ENST00000596984.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4573
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33030
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16079
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2076
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu15Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/19-8509928-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509928
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509928
    reference: chr 19
allele count: 1
allele frequency: 5.068423720223011e-5
allele num: 19730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.46A>C
  hgvsp: ENSP00000471530.1:p.Ile16Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.46A>C
  hgvsp: ENSP00000470017.1:p.Ile16Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.46A>C
  hgvsp: ENSP00000472789.1:p.Ile16Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.46A>C
  hgvsp: ENSP00000325376.2:p.Ile16Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.46A>C
  hgvsp: ENSP00000325732.2:p.Ile16Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.46A>C
  hgvsp: ENSP00000471339.1:p.Ile16Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.46A>C
  hgvsp: ENSP00000470932.1:p.Ile16Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.125A>C
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33119
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15994
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15535
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32548
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile16Leu
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP

19-8509932-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509932
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509932
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 19768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.50A>G
  hgvsp: ENSP00000472789.1:p.Lys17Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.50A>G
  hgvsp: ENSP00000470017.1:p.Lys17Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.129A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.50A>G
  hgvsp: ENSP00000471339.1:p.Lys17Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.50A>G
  hgvsp: ENSP00000470932.1:p.Lys17Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.50A>G
  hgvsp: ENSP00000325376.2:p.Lys17Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.50A>G
  hgvsp: ENSP00000325732.2:p.Lys17Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.50A>G
  hgvsp: ENSP00000471530.1:p.Lys17Arg
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16292
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32720
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2148
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Lys17Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-8509941-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509941
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509941
    reference: chr 19
allele count: 1
allele frequency: 5.158893933140735e-5
allele num: 19384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.59A>C
  hgvsp: ENSP00000470932.1:p.Glu20Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.59A>C
  hgvsp: ENSP00000325732.2:p.Glu20Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.59A>C
  hgvsp: ENSP00000470017.1:p.Glu20Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.59A>C
  hgvsp: ENSP00000472789.1:p.Glu20Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.138A>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.59A>C
  hgvsp: ENSP00000325376.2:p.Glu20Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.59A>C
  hgvsp: ENSP00000471530.1:p.Glu20Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.59A>C
  hgvsp: ENSP00000471339.1:p.Glu20Ala
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17639
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17339
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30918
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.75e1
  variant carriers: 1
hgvs: p.Glu20Ala
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

19-8509943-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509943
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509943
    reference: chr 19
allele count: 1
allele frequency: 5.231767290990897e-5
allele num: 19114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.61G>A
  hgvsp: ENSP00000472789.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.61G>A
  hgvsp: ENSP00000325376.2:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.61G>A
  hgvsp: ENSP00000471339.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.61G>A
  hgvsp: ENSP00000470017.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.61G>A
  hgvsp: ENSP00000325732.2:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.140G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.61G>A
  hgvsp: ENSP00000470932.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.61G>A
  hgvsp: ENSP00000471530.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18052
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30327
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2922
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2362
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu21Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

19-8509949-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509949
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509949
    reference: chr 19
allele count: 1
allele frequency: 5.577867023650156e-5
allele num: 17928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.67G>T
  hgvsp: ENSP00000471530.1:p.Gly23Cys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.67G>T
  hgvsp: ENSP00000471339.1:p.Gly23Cys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.67G>T
  hgvsp: ENSP00000325732.2:p.Gly23Cys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.67G>T
  hgvsp: ENSP00000472789.1:p.Gly23Cys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.146G>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.67G>T
  hgvsp: ENSP00000470017.1:p.Gly23Cys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.67G>T
  hgvsp: ENSP00000470932.1:p.Gly23Cys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.67G>T
  hgvsp: ENSP00000325376.2:p.Gly23Cys
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19533
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29635
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27653
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly23Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

19-8509951-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509951
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509951
    reference: chr 19
allele count: 16
allele frequency: 8.860338907963229e-4
allele num: 18058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.69C>T
  hgvsp: ENST00000601645.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.148C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.69C>T
  hgvsp: ENST00000600092.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.69C>T
  hgvsp: ENST00000348943.3:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.69C>T
  hgvsp: ENST00000594907.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.69C>T
  hgvsp: ENST00000596984.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.69C>T
  hgvsp: ENST00000325495.4:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.69C>T
  hgvsp: ENST00000600806.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29680
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28327
  bin: 2.25e1
  variant carriers: 2
hgvs: p.Gly23Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

19-8509958-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509958
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509958
    reference: chr 19
allele count: 6
allele frequency: 3.434065934065934e-4
allele num: 17472
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.76G>A
  hgvsp: ENSP00000325376.2:p.Gly26Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.76G>A
  hgvsp: ENSP00000470932.1:p.Gly26Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.76G>A
  hgvsp: ENSP00000471339.1:p.Gly26Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.76G>A
  hgvsp: ENSP00000472789.1:p.Gly26Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.76G>A
  hgvsp: ENSP00000471530.1:p.Gly26Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.155G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.76G>A
  hgvsp: ENSP00000325732.2:p.Gly26Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.76G>A
  hgvsp: ENSP00000470017.1:p.Gly26Ser
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20887
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28423
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5133
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly26Ser
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: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

19-8509965-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509965
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509965
    reference: chr 19
allele count: 8
allele frequency: 4.828585224529213e-4
allele num: 16568
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.83C>T
  hgvsp: ENSP00000470932.1:p.Pro28Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.83C>T
  hgvsp: ENSP00000470017.1:p.Pro28Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.83C>T
  hgvsp: ENSP00000325376.2:p.Pro28Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.83C>T
  hgvsp: ENSP00000471339.1:p.Pro28Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.83C>T
  hgvsp: ENSP00000325732.2:p.Pro28Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.83C>T
  hgvsp: ENSP00000472789.1:p.Pro28Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.162C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.83C>T
  hgvsp: ENSP00000471530.1:p.Pro28Leu
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25829
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro28Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

19-8509974-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509974
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509974
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 15466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.92A>G
  hgvsp: ENSP00000471530.1:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.92A>G
  hgvsp: ENSP00000471339.1:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.92A>G
  hgvsp: ENSP00000470932.1:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.92A>G
  hgvsp: ENSP00000470017.1:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.171A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.92A>G
  hgvsp: ENSP00000325732.2:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.92A>G
  hgvsp: ENSP00000325376.2:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.92A>G
  hgvsp: ENSP00000472789.1:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22817
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22323
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1207
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asn31Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

19-8509975-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509975
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509975
    reference: chr 19
allele count: 4
allele frequency: 2.787068004459309e-4
allele num: 14352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.93C>T
  hgvsp: ENST00000348943.3:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.93C>T
  hgvsp: ENST00000325495.4:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.93C>T
  hgvsp: ENST00000596984.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.93C>T
  hgvsp: ENST00000600092.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.172C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.93C>T
  hgvsp: ENST00000600806.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.93C>T
  hgvsp: ENST00000594907.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.93C>T
  hgvsp: ENST00000601645.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21434
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19684
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn31Asn
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

19-8509976-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509976
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509976
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 14338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.94G>T
  hgvsp: ENSP00000472789.1:p.Gly32Trp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.94G>T
  hgvsp: ENSP00000470932.1:p.Gly32Trp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.94G>T
  hgvsp: ENSP00000325376.2:p.Gly32Trp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.173G>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.94G>T
  hgvsp: ENSP00000471530.1:p.Gly32Trp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.94G>T
  hgvsp: ENSP00000470017.1:p.Gly32Trp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.94G>T
  hgvsp: ENSP00000471339.1:p.Gly32Trp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.94G>T
  hgvsp: ENSP00000325732.2:p.Gly32Trp
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21431
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1915
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Gly32Trp
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: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP

19-8509978-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509978
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509978
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 14358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.96G>T
  hgvsp: ENST00000594907.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.96G>T
  hgvsp: ENST00000601645.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.175G>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.96G>T
  hgvsp: ENST00000600092.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.96G>T
  hgvsp: ENST00000596984.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.96G>T
  hgvsp: ENST00000600806.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.96G>T
  hgvsp: ENST00000348943.3:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.96G>T
  hgvsp: ENST00000325495.4:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27836
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21187
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1208
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27626
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Gly32Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP

19-8509984-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509984
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509984
    reference: chr 19
allele count: 1
allele frequency: 8.252186829509821e-5
allele num: 12118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.102G>A
  hgvsp: ENST00000594907.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.102G>A
  hgvsp: ENST00000600806.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.102G>A
  hgvsp: ENST00000325495.4:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.102G>A
  hgvsp: ENST00000600092.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.102G>A
  hgvsp: ENST00000596984.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.102G>A
  hgvsp: ENST00000348943.3:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.181G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.102G>A
  hgvsp: ENST00000601645.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17448
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31092
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1272
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro34Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

19-8509988-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509988
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509988
    reference: chr 19
allele count: 1
allele frequency: 8.29324929507381e-5
allele num: 12058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.106C>G
  hgvsp: ENSP00000472789.1:p.Pro36Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.106C>G
  hgvsp: ENSP00000470017.1:p.Pro36Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.106C>G
  hgvsp: ENSP00000471530.1:p.Pro36Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.106C>G
  hgvsp: ENSP00000470932.1:p.Pro36Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.106C>G
  hgvsp: ENSP00000325376.2:p.Pro36Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.106C>G
  hgvsp: ENSP00000471339.1:p.Pro36Ala
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.185C>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.106C>G
  hgvsp: ENSP00000325732.2:p.Pro36Ala
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16963
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1697
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15763
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro36Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

19-8509989-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509989
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509989
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 11836
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.107C>T
  hgvsp: ENSP00000325732.2:p.Pro36Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.107C>T
  hgvsp: ENSP00000470932.1:p.Pro36Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.107C>T
  hgvsp: ENSP00000471530.1:p.Pro36Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.107C>T
  hgvsp: ENSP00000472789.1:p.Pro36Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.107C>T
  hgvsp: ENSP00000325376.2:p.Pro36Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.107C>T
  hgvsp: ENSP00000470017.1:p.Pro36Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.107C>T
  hgvsp: ENSP00000471339.1:p.Pro36Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.186C>T
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32058
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16510
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15378
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro36Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

19-8509994-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509994
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509994
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 11028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.112G>A
  hgvsp: ENSP00000470932.1:p.Gly38Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.112G>A
  hgvsp: ENSP00000471339.1:p.Gly38Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.112G>A
  hgvsp: ENSP00000325376.2:p.Gly38Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.112G>A
  hgvsp: ENSP00000325732.2:p.Gly38Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.112G>A
  hgvsp: ENSP00000470017.1:p.Gly38Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.112G>A
  hgvsp: ENSP00000472789.1:p.Gly38Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.112G>A
  hgvsp: ENSP00000471530.1:p.Gly38Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.191G>A
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33344
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32473
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1752
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly38Ser
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

19-8509995-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8509995
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8509995
    reference: chr 19
allele count: 1
allele frequency: 9.152480322167308e-5
allele num: 10926
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.113G>A
  hgvsp: ENSP00000470932.1:p.Gly38Asp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.113G>A
  hgvsp: ENSP00000471530.1:p.Gly38Asp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.113G>A
  hgvsp: ENSP00000325732.2:p.Gly38Asp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.113G>A
  hgvsp: ENSP00000472789.1:p.Gly38Asp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.113G>A
  hgvsp: ENSP00000470017.1:p.Gly38Asp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.113G>A
  hgvsp: ENSP00000471339.1:p.Gly38Asp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.192G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.113G>A
  hgvsp: ENSP00000325376.2:p.Gly38Asp
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33586
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly38Asp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

19-8510019-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8510019
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8510019
    reference: chr 19
allele count: 1
allele frequency: 1.176470588235294e-4
allele num: 8500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.113+24C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.113+24C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.192+24C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.113+24C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.113+24C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.113+24C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.113+24C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.113+24C>T
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34782
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8941
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 2.75e1
  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: 2287
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7709
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3388
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

19-8510031-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8510031
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8510031
    reference: chr 19
allele count: 1
allele frequency: 1.355380862022228e-4
allele num: 7378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.113+36T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.113+36T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.113+36T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.113+36T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.113+36T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.113+36T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.192+36T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.113+36T>C
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 947
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

19-8510038-CCGCGGCCGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8510038
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8510029
    reference: chr 19
allele count: 1
allele frequency: 1.533272002453235e-4
allele num: 6522
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2417
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3462
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24410
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9054
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: CCGCGGCCGA
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

19-8510045-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8510045
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8510045
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 5832
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.113+50C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.113+50C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.113+50C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.113+50C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.113+50C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.192+50C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.113+50C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.113+50C>T
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32387
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  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: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2452
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20765
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

19-8520238-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520238
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520238
    reference: chr 19
allele count: 1
allele frequency: 8.584575235217362e-6
allele num: 116488
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.193-51T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.114-51T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.114-51T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.114-51T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.114-51T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.114-51T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.114-51T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.114-51T>G
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14230
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1537
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1209
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1805
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6430
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7765
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1686
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-8520240-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520240
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520240
    reference: chr 19
allele count: 1
allele frequency: 8.589736982253604e-6
allele num: 116418
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.114-49G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.114-49G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.114-49G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.114-49G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.114-49G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.114-49G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.114-49G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.193-49G>A
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7754
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2903
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3972
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1982
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2150
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3212
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

19-8520245-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520245
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520245
    reference: chr 19
allele count: 1
allele frequency: 8.573976267233693e-6
allele num: 116632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.114-44G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.193-44G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.114-44G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.114-44G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.114-44G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.114-44G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.114-44G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.114-44G>A
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3116
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2053
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2026
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1350
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

19-8520248-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520248
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520248
    reference: chr 19
allele count: 1
allele frequency: 8.560031500915923e-6
allele num: 116822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.114-41A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.114-41A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.114-41A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.114-41A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.114-41A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.114-41A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.114-41A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.193-41A>G
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2241
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1362
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2037
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1934
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP

19-8520260-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520260
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520260
    reference: chr 19
allele count: 1
allele frequency: 8.494011721736177e-6
allele num: 117730
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.114-29T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.114-29T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.114-29T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.114-29T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.114-29T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.114-29T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.114-29T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.193-29T>G
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27155
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7051
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3166
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD

19-8520261-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520261
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520261
    reference: chr 19
allele count: 1
allele frequency: 8.485506754463376e-6
allele num: 117848
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.114-28A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.114-28A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.114-28A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.193-28A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.114-28A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.114-28A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.114-28A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.114-28A>G
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3171
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2007
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1849
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

19-8520263-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520263
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520262
    reference: chr 19
allele count: 362
allele frequency: 3.075981850007647e-3
allele num: 117686
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.114-19delT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.114-19delT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.193-19delT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.114-19delT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.114-19delT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.114-19delT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.114-19delT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.114-19delT
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20046
  bin: 2.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 4710
  bin: 3.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 5.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 3.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 4.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15455
  bin: 2.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26650
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 1
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: CT
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

19-8520271-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520271
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520271
    reference: chr 19
allele count: 1
allele frequency: 8.382370198997468e-6
allele num: 119298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.114-18C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.114-18C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.114-18C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.193-18C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.114-18C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.114-18C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.114-18C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.114-18C>T
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9239
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29367
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1050
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7263
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4089
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

19-8520276-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520276
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520276
    reference: chr 19
allele count: 1
allele frequency: 8.335556148306214e-6
allele num: 119968
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.114-13C>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.114-13C>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.114-13C>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.114-13C>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.114-13C>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.193-13C>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.114-13C>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.114-13C>G
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2025
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
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: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-8520278-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520278
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520278
    reference: chr 19
allele count: 1
allele frequency: 8.319190709127816e-6
allele num: 120204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.114-11C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.193-11C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.114-11C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.114-11C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.114-11C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.114-11C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.114-11C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.114-11C>T
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7341
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3207
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7819
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

19-8520279-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520279
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520279
    reference: chr 19
allele count: 23
allele frequency: 1.911823380768719e-4
allele num: 120304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.114-10T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.114-10T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.114-10T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.114-10T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.114-10T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.114-10T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.114-10T>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.193-10T>G
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21984
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16649
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9280
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4663
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30547
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4115
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3207
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7838
  bin: 9.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

19-8520280-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520280
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520280
    reference: chr 19
allele count: 5
allele frequency: 4.15337586390218e-5
allele num: 120384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.114-9C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.193-9C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.114-9C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.114-9C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.114-9C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.114-9C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.114-9C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.114-9C>T
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9307
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3051
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7344
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2023
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

19-8520298-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520298
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520298
    reference: chr 19
allele count: 1
allele frequency: 8.259820927082301e-6
allele num: 121068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.123A>T
  hgvsp: ENSP00000325732.2:p.Glu41Asp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.123A>T
  hgvsp: ENSP00000471339.1:p.Glu41Asp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.202A>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.123A>T
  hgvsp: ENSP00000470932.1:p.Glu41Asp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.123A>T
  hgvsp: ENSP00000471530.1:p.Glu41Asp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.123A>T
  hgvsp: ENSP00000470017.1:p.Glu41Asp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.123A>T
  hgvsp: ENSP00000472789.1:p.Glu41Asp
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.123A>T
  hgvsp: ENSP00000325376.2:p.Glu41Asp
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2026
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7407
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu41Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP

19-8520303-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520303
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520303
    reference: chr 19
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.128C>T
  hgvsp: ENSP00000470932.1:p.Pro43Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.128C>T
  hgvsp: ENSP00000472789.1:p.Pro43Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.128C>T
  hgvsp: ENSP00000471339.1:p.Pro43Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.128C>T
  hgvsp: ENSP00000471530.1:p.Pro43Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.207C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.128C>T
  hgvsp: ENSP00000325376.2:p.Pro43Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.128C>T
  hgvsp: ENSP00000470017.1:p.Pro43Leu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.128C>T
  hgvsp: ENSP00000325732.2:p.Pro43Leu
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7415
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7820
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro43Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

19-8520318-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520318
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520318
    reference: chr 19
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.143A>G
  hgvsp: ENSP00000470017.1:p.Lys48Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.143A>G
  hgvsp: ENSP00000471339.1:p.Lys48Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.143A>G
  hgvsp: ENSP00000471530.1:p.Lys48Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.143A>G
  hgvsp: ENSP00000325732.2:p.Lys48Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.143A>G
  hgvsp: ENSP00000325376.2:p.Lys48Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.143A>G
  hgvsp: ENSP00000470932.1:p.Lys48Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.222A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.143A>G
  hgvsp: ENSP00000472789.1:p.Lys48Arg
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7822
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys48Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

19-8520324-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520324
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520324
    reference: chr 19
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.228A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.149A>G
  hgvsp: ENSP00000325732.2:p.Lys50Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.149A>G
  hgvsp: ENSP00000471339.1:p.Lys50Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.149A>G
  hgvsp: ENSP00000471530.1:p.Lys50Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.149A>G
  hgvsp: ENSP00000472789.1:p.Lys50Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.149A>G
  hgvsp: ENSP00000470017.1:p.Lys50Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.149A>G
  hgvsp: ENSP00000470932.1:p.Lys50Arg
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.149A>G
  hgvsp: ENSP00000325376.2:p.Lys50Arg
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31469
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys50Arg
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-8520331-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520331
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520331
    reference: chr 19
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.156A>G
  hgvsp: ENST00000600806.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.156A>G
  hgvsp: ENST00000594907.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.156A>G
  hgvsp: ENST00000325495.4:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.235A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.156A>G
  hgvsp: ENST00000600092.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.156A>G
  hgvsp: ENST00000601645.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.156A>G
  hgvsp: ENST00000596984.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.156A>G
  hgvsp: ENST00000348943.3:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9386
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3222
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7822
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Lys52Lys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS

19-8520351-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520351
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520351
    reference: chr 19
allele count: 15
allele frequency: 1.235930985613763e-4
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.176A>G
  hgvsp: ENSP00000470932.1:p.Asn59Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.255A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.176A>G
  hgvsp: ENSP00000471339.1:p.Asn59Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.176A>G
  hgvsp: ENSP00000325376.2:p.Asn59Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.176A>G
  hgvsp: ENSP00000471530.1:p.Asn59Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.176A>G
  hgvsp: ENSP00000325732.2:p.Asn59Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.176A>G
  hgvsp: ENSP00000470017.1:p.Asn59Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.176A>G
  hgvsp: ENSP00000472789.1:p.Asn59Ser
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1391
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31508
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn59Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-8520372-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520372
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520372
    reference: chr 19
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.197A>G
  hgvsp: ENSP00000470932.1:p.Asn66Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.197A>G
  hgvsp: ENSP00000472789.1:p.Asn66Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.197A>G
  hgvsp: ENSP00000470017.1:p.Asn66Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.197A>G
  hgvsp: ENSP00000471530.1:p.Asn66Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.197A>G
  hgvsp: ENSP00000325376.2:p.Asn66Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.197A>G
  hgvsp: ENSP00000325732.2:p.Asn66Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.276A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.197A>G
  hgvsp: ENSP00000471339.1:p.Asn66Ser
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4129
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7825
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn66Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-8520376-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520376
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520376
    reference: chr 19
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.201A>G
  hgvsp: ENST00000325495.4:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.201A>G
  hgvsp: ENST00000600806.1:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.201A>G
  hgvsp: ENST00000601645.1:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.201A>G
  hgvsp: ENST00000600092.1:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.201A>G
  hgvsp: ENST00000596984.1:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.201A>G
  hgvsp: ENST00000348943.3:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.280A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.201A>G
  hgvsp: ENST00000594907.1:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31510
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4130
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro67Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

19-8520380-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520380
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520380
    reference: chr 19
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.205A>G
  hgvsp: ENSP00000471530.1:p.Lys69Glu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.205A>G
  hgvsp: ENSP00000470932.1:p.Lys69Glu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.284A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.205A>G
  hgvsp: ENSP00000470017.1:p.Lys69Glu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.205A>G
  hgvsp: ENSP00000325732.2:p.Lys69Glu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.205A>G
  hgvsp: ENSP00000325376.2:p.Lys69Glu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.205A>G
  hgvsp: ENSP00000471339.1:p.Lys69Glu
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.205A>G
  hgvsp: ENSP00000472789.1:p.Lys69Glu
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7455
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys69Glu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

19-8520385-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520385
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520385
    reference: chr 19
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.210A>T
  hgvsp: ENSP00000325732.2:p.Arg70Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.210A>T
  hgvsp: ENSP00000471530.1:p.Arg70Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.210A>T
  hgvsp: ENSP00000325376.2:p.Arg70Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.210A>T
  hgvsp: ENSP00000470932.1:p.Arg70Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.210A>T
  hgvsp: ENSP00000471339.1:p.Arg70Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.210A>T
  hgvsp: ENSP00000470017.1:p.Arg70Ser
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.289A>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.210A>T
  hgvsp: ENSP00000472789.1:p.Arg70Ser
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg70Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

19-8520389-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520389
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520389
    reference: chr 19
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.214A>G
  hgvsp: ENSP00000325376.2:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.214A>G
  hgvsp: ENSP00000471530.1:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.293A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.214A>G
  hgvsp: ENSP00000325732.2:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.214A>G
  hgvsp: ENSP00000470932.1:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.214A>G
  hgvsp: ENSP00000471339.1:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.214A>G
  hgvsp: ENSP00000470017.1:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.214A>G
  hgvsp: ENSP00000472789.1:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1395
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg72Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

19-8520394-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520394
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520394
    reference: chr 19
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.219C>G
  hgvsp: ENST00000325495.4:c.219C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.219C>G
  hgvsp: ENST00000600806.1:c.219C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.219C>G
  hgvsp: ENST00000600092.1:c.219C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.298C>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.219C>G
  hgvsp: ENST00000596984.1:c.219C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.219C>G
  hgvsp: ENST00000601645.1:c.219C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.219C>G
  hgvsp: ENST00000348943.3:c.219C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.219C>G
  hgvsp: ENST00000594907.1:c.219C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7457
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala73Ala
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum

19-8520394-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520394
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520394
    reference: chr 19
allele count: 3
allele frequency: 2.471413978317461e-5
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.219C>T
  hgvsp: ENST00000600806.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.219C>T
  hgvsp: ENST00000325495.4:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.219C>T
  hgvsp: ENST00000348943.3:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.219C>T
  hgvsp: ENST00000596984.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.219C>T
  hgvsp: ENST00000601645.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.219C>T
  hgvsp: ENST00000594907.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.298C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.219C>T
  hgvsp: ENST00000600092.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31505
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7828
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala73Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-8520436-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520436
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520436
    reference: chr 19
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.261T>C
  hgvsp: ENST00000596984.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.261T>C
  hgvsp: ENST00000601645.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.261T>C
  hgvsp: ENST00000600806.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.261T>C
  hgvsp: ENST00000600092.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.261T>C
  hgvsp: ENST00000594907.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.261T>C
  hgvsp: ENST00000348943.3:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.261T>C
  hgvsp: ENST00000325495.4:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.340T>C
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31396
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3076
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7447
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu87Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff

19-8520442-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520442
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520442
    reference: chr 19
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.267C>T
  hgvsp: ENST00000594907.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.267C>T
  hgvsp: ENST00000325495.4:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.267C>T
  hgvsp: ENST00000596984.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.267C>T
  hgvsp: ENST00000600092.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.267C>T
  hgvsp: ENST00000601645.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.267C>T
  hgvsp: ENST00000600806.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.267C>T
  hgvsp: ENST00000348943.3:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.346C>T
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2033
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp89Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

19-8520452-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520452
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520452
    reference: chr 19
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.277G>A
  hgvsp: ENSP00000470932.1:p.Glu93Lys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.356G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.277G>A
  hgvsp: ENSP00000325732.2:p.Glu93Lys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.277G>A
  hgvsp: ENSP00000470017.1:p.Glu93Lys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.277G>A
  hgvsp: ENSP00000472789.1:p.Glu93Lys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.277G>A
  hgvsp: ENSP00000471530.1:p.Glu93Lys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.277G>A
  hgvsp: ENSP00000325376.2:p.Glu93Lys
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.277G>A
  hgvsp: ENSP00000471339.1:p.Glu93Lys
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31034
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1391
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3070
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu93Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

19-8520474-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520474
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520475
    reference: chr 19
allele count: 1
allele frequency: 8.30937463646486e-6
allele num: 120346
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.362+18dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.283+18dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.283+18dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.283+18dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.283+18dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.283+18dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.283+18dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.283+18dupT
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7820
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-8520475-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520475
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520475
    reference: chr 19
allele count: 1
allele frequency: 8.312966565248474e-6
allele num: 120294
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.283+17T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.283+17T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.283+17T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.283+17T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.283+17T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.362+17T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.283+17T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.283+17T>C
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1388
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4090
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3028
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ

19-8520479-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520479
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520479
    reference: chr 19
allele count: 9
allele frequency: 7.48652425633859e-5
allele num: 120216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.283+21G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.283+21G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.283+21G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.283+21G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.283+21G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.362+21G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.283+21G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.283+21G>C
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16707
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9243
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7827
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 7133
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ

19-8520484-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520484
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520484
    reference: chr 19
allele count: 1
allele frequency: 8.329168748958854e-6
allele num: 120060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.283+26G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.283+26G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.283+26G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.283+26G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.283+26G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.283+26G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.283+26G>A
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.362+26G>A
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2024
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4061
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2048
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

19-8520485-T-TGAGAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520485
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520490
    reference: chr 19
allele count: 1
allele frequency: 8.332361224523806e-6
allele num: 120014
alternate allele: TGAGAA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.362+29_362+33dupAGAAG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.283+29_283+33dupAGAAG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.283+29_283+33dupAGAAG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.283+29_283+33dupAGAAG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.283+29_283+33dupAGAAG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.283+29_283+33dupAGAAG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.283+29_283+33dupAGAAG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.283+29_283+33dupAGAAG
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9114
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1367
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25880
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6928
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3194
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

19-8520501-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520501
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520501
    reference: chr 19
allele count: 1
allele frequency: 8.388839487945237e-6
allele num: 119206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.362+43T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.283+43T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.283+43T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.283+43T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.283+43T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.283+43T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.283+43T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.283+43T>C
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7013
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6144
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17371
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3195
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7816
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD

19-8520503-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520503
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520504
    reference: chr 19
allele count: 4
allele frequency: 3.357338302194021e-5
allele num: 119142
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.283+46dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.283+46dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.362+46dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.283+46dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.283+46dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.283+46dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.283+46dupT
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.283+46dupT
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13067
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8588
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6979
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3294
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2829
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7819
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD

19-8520504-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520504
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520504
    reference: chr 19
allele count: 1
allele frequency: 8.400255367763179e-6
allele num: 119044
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.283+46T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.283+46T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.283+46T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.283+46T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.362+46T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.283+46T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.283+46T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.283+46T>C
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16061
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2827
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6063
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2505
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

19-8520508-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8520508
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8520508
    reference: chr 19
allele count: 1
allele frequency: 8.429570934839416e-6
allele num: 118630
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.283+50T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.283+50T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.283+50T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.283+50T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.283+50T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.283+50T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.362+50T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.283+50T>C
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3909
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5773
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1997
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1370
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2871
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

19-8527381-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8527381
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8527381
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.284-32G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.284-32G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.284-32G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.284-32G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.284-1000G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.284-1000G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000593293
  gene symbol: HNRNPM
  hgvsc: ENST00000593293.1:n.529G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.363-1000G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.284-32G>C
  variant of: http://identifiers.org/hgnc/5046
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25184
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

19-8527385-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8527385
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8527385
    reference: chr 19
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.284-996T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.363-996T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.284-28T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.284-28T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.284-28T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000593293
  gene symbol: HNRNPM
  hgvsc: ENST00000593293.1:n.533T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.284-996T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.284-28T>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.284-28T>C
  variant of: http://identifiers.org/hgnc/5046
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25183
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

19-8527426-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8527426
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8527426
    reference: chr 19
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.284-955A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000593293
  gene symbol: HNRNPM
  hgvsc: ENST00000593293.1:n.574A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.297A>G
  hgvsp: ENST00000325495.4:c.297A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.363-955A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.297A>G
  hgvsp: ENST00000600092.1:c.297A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.297A>G
  hgvsp: ENST00000348943.3:c.297A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.297A>G
  hgvsp: ENST00000594907.1:c.297A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.284-955A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.297A>G
  hgvsp: ENST00000601645.1:c.297A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25184
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr99Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ

19-8527447-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8527447
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8527447
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.318C>T
  hgvsp: ENST00000601645.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.363-934C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.284-934C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.318C>T
  hgvsp: ENST00000600092.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000593293
  gene symbol: HNRNPM
  hgvsc: ENST00000593293.1:n.595C>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.318C>T
  hgvsp: ENST00000594907.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.318C>T
  hgvsp: ENST00000325495.4:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.318C>T
  hgvsp: ENST00000348943.3:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.284-934C>T
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25182
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp106Asp
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-8527470-GTGTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8527470
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8527466
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000593293
  gene symbol: HNRNPM
  hgvsc: ENST00000593293.1:n.613+8_613+11delTCTG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.336+8_336+11delTCTG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.336+8_336+11delTCTG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.336+8_336+11delTCTG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.336+8_336+11delTCTG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.284-908_284-905delTCTG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.284-908_284-905delTCTG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.336+8_336+11delTCTG
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.363-908_363-905delTCTG
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25183
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: c.336+8_336+11delTCTG
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: GTGTC
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

19-8527479-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8527479
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8527479
    reference: chr 19
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.336+14A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.284-902A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000593293
  gene symbol: HNRNPM
  hgvsc: ENST00000593293.1:n.613+14A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.336+14A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.336+14A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.284-902A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.363-902A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.336+14A>G
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.336+14A>G
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25183
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55923
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

19-8527480-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8527480
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8527480
    reference: chr 19
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.336+15G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.336+15G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.284-901G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.336+15G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000593293
  gene symbol: HNRNPM
  hgvsc: ENST00000593293.1:n.613+15G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.284-901G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.336+15G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.363-901G>C
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.336+15G>C
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25183
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

19-8527480-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8527480
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 8527480
    reference: chr 19
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471530
  ensembl transcript: ENST00000600806
  gene symbol: HNRNPM
  hgvsc: ENST00000600806.1:c.284-901G>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000593293
  gene symbol: HNRNPM
  hgvsc: ENST00000593293.1:n.613+15G>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470932
  ensembl transcript: ENST00000600092
  gene symbol: HNRNPM
  hgvsc: ENST00000600092.1:c.336+15G>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325376
  ensembl transcript: ENST00000325495
  gene symbol: HNRNPM
  hgvsc: ENST00000325495.4:c.336+15G>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000470017
  ensembl transcript: ENST00000596984
  gene symbol: HNRNPM
  hgvsc: ENST00000596984.1:c.284-901G>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000471339
  ensembl transcript: ENST00000601645
  gene symbol: HNRNPM
  hgvsc: ENST00000601645.1:c.336+15G>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000472789
  ensembl transcript: ENST00000594907
  gene symbol: HNRNPM
  hgvsc: ENST00000594907.1:c.336+15G>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl transcript: ENST00000597813
  gene symbol: HNRNPM
  hgvsc: ENST00000597813.1:n.363-901G>T
  variant of: http://identifiers.org/hgnc/5046
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099783
  ensembl protein: ENSP00000325732
  ensembl transcript: ENST00000348943
  gene symbol: HNRNPM
  hgvsc: ENST00000348943.3:c.336+15G>T
  variant of: http://identifiers.org/hgnc/5046
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25183
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 375
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32000
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3682
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1898
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.5e-2

DP
type: SiteQuality
SIO_000300: 4.61869e5

FS
type: SiteQuality
SIO_000300: 4.365e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.531e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
all individuals: 839
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1762
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32509
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 138
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1281
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.208333333333333e-4
allele num: 1920
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11942
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 918
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.11e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.349e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.96e-1

DP
type: SiteQuality
SIO_000300: 4.65117e5

GenotypeQuality
all individuals: 816
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15422
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1701
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 56
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3884
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12034
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2818
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1374
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.192107995846313e-4
allele num: 1926
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.36e-1

DP
type: SiteQuality
SIO_000300: 4.66817e5

VQSLOD
type: SiteQuality
SIO_000300: -2.99e0

QD
type: SiteQuality
SIO_000300: 2.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.11e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQRankSum
type: SiteQuality
SIO_000300: -1.599e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQ
type: SiteQuality
SIO_000300: 5.843e1

GenotypeQuality
all individuals: 98
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1887
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3876
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
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: 0
allele frequency: 0.0e0
allele num: 12154
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1980
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2852
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.66429e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

QD
type: SiteQuality
SIO_000300: 9.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.425e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.08e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 178
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32385
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15620
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3710
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.260366760284156e-5
allele num: 12106
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1964
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 912
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1400
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.65041e5

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.11e-2

FS
type: SiteQuality
SIO_000300: 8.960000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.186e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.135e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.666e0

VQSLOD
type: SiteQuality
SIO_000300: -8.898e-1

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1056
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3774
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2870
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 932
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1978
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12160
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.102272727272727e-4
allele num: 1408
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.09e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 8.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.253e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 1.778e0

DP
type: SiteQuality
SIO_000300: 4.65693e5

GenotypeQuality
all individuals: 400
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15901
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1164
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 97
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32270
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3638
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 940
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1468
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.13e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.35e0

MQRankSum
type: SiteQuality
SIO_000300: -1.666e0

QD
type: SiteQuality
SIO_000300: 1.559e1

DP
type: SiteQuality
SIO_000300: 4.64292e5

MQ
type: SiteQuality
SIO_000300: 5.572e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

GenotypeQuality
all individuals: 648
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 151
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2265
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2836
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1942
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.474576271186441e-5
allele num: 11800
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.677e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

MQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.49989e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.44e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.9e-2

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
all individuals: 1319
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 811
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17776
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11632
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.263157894736842e-4
allele num: 1900
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.91e-1

FS
type: SiteQuality
SIO_000300: 2.218e0

DP
type: SiteQuality
SIO_000300: 4.45164e5

MQ
type: SiteQuality
SIO_000300: 5.863e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.845e0

MQRankSum
type: SiteQuality
SIO_000300: 3.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.843e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.53e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.528e0

QD
type: SiteQuality
SIO_000300: 1.156e1

GenotypeQuality
all individuals: 96
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19182
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2278
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3445
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 782
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 236
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.762227238525207e-4
allele num: 2658
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1776
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10832
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.87e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-1

DP
type: SiteQuality
SIO_000300: 4.27692e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.077e1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 7.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
all individuals: 19249
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2833
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 76
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 52
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 95
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 335
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 23
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 322
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2676
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 1.468968049944914e-3
allele num: 10892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 104
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

QD
type: SiteQuality
SIO_000300: 1.24e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

FS
type: SiteQuality
SIO_000300: 1.889e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-2

DP
type: SiteQuality
SIO_000300: 4.28204e5

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 20790
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27549
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1319
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2434
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 9.75e1
variant carriers: 7

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 3.472222222222222e-3
allele num: 1728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 98
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.18e-2

FS
type: SiteQuality
SIO_000300: 1.5106e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

DP
type: SiteQuality
SIO_000300: 4.16314e5

QD
type: SiteQuality
SIO_000300: 7.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.537e0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 294
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2664
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24792
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2034
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23150
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 84
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.03777501037775e-4
allele num: 9636
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 2.8e-3
allele num: 2500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.94e-1

QD
type: SiteQuality
SIO_000300: 1.444e1

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.67e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

FS
type: SiteQuality
SIO_000300: 1.224e0

DP
type: SiteQuality
SIO_000300: 3.963e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 5.855e1

GenotypeQuality
all individuals: 579
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1889
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26213
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1976
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 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: 8738
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.057e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 3.70944e5

FS
type: SiteQuality
SIO_000300: 4.374e0

QD
type: SiteQuality
SIO_000300: 1.174e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.16e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 1337
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 686
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27089
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1837
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 562
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 106
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2696
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1368
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.092050209205021e-3
allele num: 1912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7988
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.685e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 1.314e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

DP
type: SiteQuality
SIO_000300: 3.59088e5

GenotypeQuality
all individuals: 1448
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1290
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27250
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20091
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1948
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1308
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2296
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7974
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.855e1

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.53e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 2.8e0

VQSLOD
type: SiteQuality
SIO_000300: -1.215e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.59028e5

GenotypeQuality
all individuals: 67
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20231
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1974
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7956
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2272
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1316
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2018
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 1.06e1

VQSLOD
type: SiteQuality
SIO_000300: -1.521e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.49e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

FS
type: SiteQuality
SIO_000300: 2.702e0

DP
type: SiteQuality
SIO_000300: 3.55862e5

GenotypeQuality
all individuals: 262
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30292
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15373
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 166
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2308
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1746
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558117793705204e-4
allele num: 6418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2056
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2048
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1048
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

FS
type: SiteQuality
SIO_000300: 1.792e0

QD
type: SiteQuality
SIO_000300: 1.15e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.509e0

DP
type: SiteQuality
SIO_000300: 3.23012e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

GenotypeQuality
all individuals: 1879
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31031
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1609
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2022
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1038
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 2.512562814070352e-3
allele num: 398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 84
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-2

QD
type: SiteQuality
SIO_000300: 1.069e1

FS
type: SiteQuality
SIO_000300: 2.797e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 3.18159e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.539e0

GenotypeQuality
all individuals: 1660
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31394
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1524
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1868
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1992
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6196
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1002
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2120
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.469999999999999e-2

DP
type: SiteQuality
SIO_000300: 3.14575e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

QD
type: SiteQuality
SIO_000300: 5.17e0

VQSLOD
type: SiteQuality
SIO_000300: -2.363e0

GenotypeQuality
all individuals: 21
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13541
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 456
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1186
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 38
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1839
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1908
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5646
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.367e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.759999999999999e-2

DP
type: SiteQuality
SIO_000300: 2.98245e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.802e0

GenotypeQuality
all individuals: 1175
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13307
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32712
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 63
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1262
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1750
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1851
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 457
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.199040767386091e-3
allele num: 834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2162
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.82e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.935e0

QD
type: SiteQuality
SIO_000300: 1.041e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-2

DP
type: SiteQuality
SIO_000300: 2.95904e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.97e-1

GenotypeQuality
all individuals: 32170
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 375
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1172
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 4.359197907585005e-4
allele num: 2294
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4054
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.232e1

MQRankSum
type: SiteQuality
SIO_000300: -1.106e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.870000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.262e0

VQSLOD
type: SiteQuality
SIO_000300: 4.02e-1

MQ
type: SiteQuality
SIO_000300: 5.652e1

DP
type: SiteQuality
SIO_000300: 2.32045e5

GenotypeQuality
all individuals: 4952
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28446
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6029
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 522
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3452
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 160
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1142
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.777777777777778e-3
allele num: 360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.44e1

VQSLOD
type: SiteQuality
SIO_000300: -1.151e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.49e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

DP
type: SiteQuality
SIO_000300: 1.99392e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1523
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 126
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 38
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1988
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1000
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.304692663582287e-4
allele num: 3026
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.05e-2

MQ
type: SiteQuality
SIO_000300: 5.396e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.21e-1

DP
type: SiteQuality
SIO_000300: 1.85137e5

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 1.3e0

QD
type: SiteQuality
SIO_000300: 4.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
all individuals: 134
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2546
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 458
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2339
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12417
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2690
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1802
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.743e1

DP
type: SiteQuality
SIO_000300: 1.81592e5

VQSLOD
type: SiteQuality
SIO_000300: 9.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.74e-2

GenotypeQuality
all individuals: 2593
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3511
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1368
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3238
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2146
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2940
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4023
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3198
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.861932938856015e-5
allele num: 10140
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64828
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14328
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
SIO_000300: -1.626e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

QD
type: SiteQuality
SIO_000300: 1.978e1

DP
type: SiteQuality
SIO_000300: 1.665174e6

FS
type: SiteQuality
SIO_000300: 8.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.227e0

GenotypeQuality
all individuals: 1207
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3143
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2622
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16005
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2875
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6426
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1973
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.788890841975742e-5
allele num: 11378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

FS
type: SiteQuality
SIO_000300: 3.864e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.989e0

QD
type: SiteQuality
SIO_000300: 1.309e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: -1.57e-1

DP
type: SiteQuality
SIO_000300: 1.669525e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
all individuals: 6546
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3907
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7746
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1149
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 924
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1319
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20203
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2894
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.863878477017163e-5
allele num: 10138
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64874
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14404
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.74e-1

DP
type: SiteQuality
SIO_000300: 1.690976e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.285e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.325e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-2

QD
type: SiteQuality
SIO_000300: 9.039999999999999e0

GenotypeQuality
all individuals: 2925
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3947
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1364
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6686
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7750
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1078
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22138
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539645881447267e-5
allele num: 64950
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.554e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.405e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.196e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 2.079e0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 1.704235e6

GenotypeQuality
all individuals: 109
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1901
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3011
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7764
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 54
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4036
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65316
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.731287022078621e-5
allele num: 14856
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.9e0

DP
type: SiteQuality
SIO_000300: 1.75526e6

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-1

QD
type: SiteQuality
SIO_000300: 8.65e0

GenotypeQuality
all individuals: 3010
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4046
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7070
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27476
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7765
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1368
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65364
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.131221719457014e-3
allele num: 884
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.372e0

QD
type: SiteQuality
SIO_000300: 1.629e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.75869e6

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.04e-1

GenotypeQuality
all individuals: 620
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 346
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1991
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3126
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6895
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1348
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8078
bin: 9.75e1
variant carriers: 358

GenotypeQuality
all individuals: 3963
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2938
bin: 7.25e1
variant carriers: 1

Other
type: Population
allele count: 3
allele frequency: 3.393665158371041e-3
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 54
allele frequency: 4.711219682428896e-3
allele num: 11462
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 7.863180656575585e-4
allele num: 10174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 275
allele frequency: 4.211203332210346e-3
allele num: 65302
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 9
allele frequency: 1.364463311097635e-3
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 8.769562871019967e-4
allele num: 14824
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.02e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.782776e6

QD
type: SiteQuality
SIO_000300: 1.192e1

VQSLOD
type: SiteQuality
SIO_000300: 5.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.01e-1

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3037
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7817
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 124
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3204
bin: 8.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51666818333485e-5
allele num: 65934
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.91e-1

QD
type: SiteQuality
SIO_000300: 1.359e1

FS
type: SiteQuality
SIO_000300: 3.189e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.592e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

DP
type: SiteQuality
SIO_000300: 1.793703e6

GenotypeQuality
all individuals: 7332
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4104
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30147
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7819
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3055
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.164686699277894e-4
allele num: 8586
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66162
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15940
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.803793e6

MQRankSum
type: SiteQuality
SIO_000300: 8.88e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.1e0

QD
type: SiteQuality
SIO_000300: 2.569e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

GenotypeQuality
all individuals: 3058
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4103
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30476
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1390
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2026
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509479531457553e-5
allele num: 66248
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16066
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -4.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.625e0

FS
type: SiteQuality
SIO_000300: 1.2258e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

MQ
type: SiteQuality
SIO_000300: 5.856e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.172e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.415e0

QD
type: SiteQuality
SIO_000300: 9.1e0

DP
type: SiteQuality
SIO_000300: 1.807373e6

GenotypeQuality
all individuals: 167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3059
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7354
bin: 6.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66284
num of homozygotes: 0

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

South Asian
type: Population
allele count: 23
allele frequency: 1.426445050855867e-3
allele num: 16124
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.25e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.823e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

DP
type: SiteQuality
SIO_000300: 1.808875e6

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

GenotypeQuality
all individuals: 1388
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3207
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 520
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4108
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7821
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 115
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30623
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.540340823405218e-5
allele num: 66310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16168
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

DP
type: SiteQuality
SIO_000300: 1.810469e6

VQSLOD
type: SiteQuality
SIO_000300: 7.09e-1

QD
type: SiteQuality
SIO_000300: 1.308e1

FS
type: SiteQuality
SIO_000300: 2.809e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.194e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
all individuals: 3232
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4120
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7820
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 31263
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3066
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1392
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

QD
type: SiteQuality
SIO_000300: 1.505e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.56e0

DP
type: SiteQuality
SIO_000300: 1.819165e6

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

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

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4127
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3226
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3067
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2027
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31323
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.373e0

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

DP
type: SiteQuality
SIO_000300: 1.820969e6

QD
type: SiteQuality
SIO_000300: 1.401e1

FS
type: SiteQuality
SIO_000300: 3.359e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

GenotypeQuality
all individuals: 7430
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3073
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31425
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3224
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4119
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.087e1

MQRankSum
type: SiteQuality
SIO_000300: -1.532e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.92e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

MQ
type: SiteQuality
SIO_000300: 5.943e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.39e0

VQSLOD
type: SiteQuality
SIO_000300: -4.977e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 1.822782e6

GenotypeQuality
all individuals: 1391
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4118
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3222
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3075
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7441
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7822
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

DP
type: SiteQuality
SIO_000300: 1.823441e6

MQ
type: SiteQuality
SIO_000300: 5.946e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.95e0

FS
type: SiteQuality
SIO_000300: 2.168e0

VQSLOD
type: SiteQuality
SIO_000300: 3.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e0

QD
type: SiteQuality
SIO_000300: 1.03e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.753e0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3079
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1392
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4123
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2031
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 31480
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7448
bin: 6.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.064000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.82395e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.509e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.843e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.852e0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4129
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3221
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7455
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7835
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 2030
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3074
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.049192122066009e-4
allele num: 66718
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 6.942837306179125e-4
allele num: 8642
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

FS
type: SiteQuality
SIO_000300: 5.17e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e0

DP
type: SiteQuality
SIO_000300: 1.825534e6

QD
type: SiteQuality
SIO_000300: 1.433e1

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e-1

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

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1394
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31505
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3080
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7457
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.198e1

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.13e-1

FS
type: SiteQuality
SIO_000300: 2.292e0

DP
type: SiteQuality
SIO_000300: 1.824897e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.892e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

GenotypeQuality
all individuals: 2031
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1394
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3081
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7824
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7457
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.68e0

MQRankSum
type: SiteQuality
SIO_000300: -4.11e-1

QD
type: SiteQuality
SIO_000300: 8.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.850000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.824938e6

FS
type: SiteQuality
SIO_000300: 5.358e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e-2

MQ
type: SiteQuality
SIO_000300: 5.94e1

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3082
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1394
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31511
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7823
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.63e-2

FS
type: SiteQuality
SIO_000300: 6.621e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.108000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 1.644e1

DP
type: SiteQuality
SIO_000300: 1.824938e6

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

GenotypeQuality
all individuals: 31510
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4131
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7458
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7824
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3082
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1394
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.933e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.142e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.99e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.73e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.27e-1

DP
type: SiteQuality
SIO_000300: 1.825038e6

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3223
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31512
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3084
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7456
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4130
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7824
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.643e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.525e0

DP
type: SiteQuality
SIO_000300: 1.825139e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.644e0

QD
type: SiteQuality
SIO_000300: 1.105e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.53e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.49e-1

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

GenotypeQuality
all individuals: 3084
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31505
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3222
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7828
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4132
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.524e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.04e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.74e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 1.825337e6

QD
type: SiteQuality
SIO_000300: 1.119e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.265e0

GenotypeQuality
all individuals: 7457
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3084
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3222
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4132
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.467406380027739e-4
allele num: 8652
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.961e1

QD
type: SiteQuality
SIO_000300: 1.119e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.04e-2

DP
type: SiteQuality
SIO_000300: 1.825337e6

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.265e0

FS
type: SiteQuality
SIO_000300: 2.524e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.73e-1

GenotypeQuality
all individuals: 1392
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 4132
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7825
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3220
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.317e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-2

MQ
type: SiteQuality
SIO_000300: 5.893e1

MQRankSum
type: SiteQuality
SIO_000300: -3.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.02e-1

DP
type: SiteQuality
SIO_000300: 1.823723e6

FS
type: SiteQuality
SIO_000300: 1.174e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

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

GenotypeQuality
all individuals: 1392
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4132
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7440
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7826
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3074
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3218
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31286
bin: 6.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.87e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 1.527e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.542e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.007e-1

DP
type: SiteQuality
SIO_000300: 1.822926e6

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

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 7825
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7422
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3214
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4123
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66606
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.98e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.1e-2

MQ
type: SiteQuality
SIO_000300: 5.885e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.107e0

VQSLOD
type: SiteQuality
SIO_000300: -6.264999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-2

QD
type: SiteQuality
SIO_000300: 9.07e0

DP
type: SiteQuality
SIO_000300: 1.820476e6

GenotypeQuality
all individuals: 3033
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4094
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29106
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3204
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7276
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16008
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66318
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

QD
type: SiteQuality
SIO_000300: 8.01e0

DP
type: SiteQuality
SIO_000300: 1.797244e6

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 5.581e0

MQRankSum
type: SiteQuality
SIO_000300: -6.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e-1

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28593
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7247
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1538
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3204
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7821
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2030
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508295625942685e-5
allele num: 66300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15984
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 8.33e-1

FS
type: SiteQuality
SIO_000300: 1.273e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.23e-1

DP
type: SiteQuality
SIO_000300: 1.792694e6

QD
type: SiteQuality
SIO_000300: 1.399e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

GenotypeQuality
all individuals: 3017
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3202
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4077
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2029
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 7
allele frequency: 6.78689160364553e-4
allele num: 10314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66258
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15948
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.73190162798753e-4
allele num: 11548
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 1.504e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.32e-1

FS
type: SiteQuality
SIO_000300: 3.006e0

MQRankSum
type: SiteQuality
SIO_000300: 4.14e-1

DP
type: SiteQuality
SIO_000300: 1.787588e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1115
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3194
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26887
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7821
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1380
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6993
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
bin: 7.25e1
variant carriers: 0

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

Other
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: 11544
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15868
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510619656182966e-5
allele num: 66198
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.236e0

QD
type: SiteQuality
SIO_000300: 7.09e0

MQRankSum
type: SiteQuality
SIO_000300: -8.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.709e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.76e-1

FS
type: SiteQuality
SIO_000300: 3.954e0

DP
type: SiteQuality
SIO_000300: 1.773452e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

GenotypeQuality
all individuals: 2024
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2968
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2190
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 219
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7821
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 222
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4059
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 2.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.314725940894166e-5
allele num: 15836
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66192
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.76514e6

MQRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 1.14e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.28e-1

GenotypeQuality
all individuals: 1532
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2014
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1371
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2775
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1590
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2544
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2830
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3932
bin: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517865274278255e-5
allele num: 65882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.713707e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.087e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 5.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.55e-1

FS
type: SiteQuality
SIO_000300: 2.681e0

MQRankSum
type: SiteQuality
SIO_000300: 5.27e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.782e1

GenotypeQuality
all individuals: 3932
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2548
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2547
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6101
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1370
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2796
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3155
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16884
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65844
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15442
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.644681839294008e-4
allele num: 8612
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.123e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-2

DP
type: SiteQuality
SIO_000300: 1.711773e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

QD
type: SiteQuality
SIO_000300: 1.211e1

GenotypeQuality
all individuals: 1558
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3917
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3371
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1369
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2835
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2882
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7816
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2012
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519664458087654e-5
allele num: 65804
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.710035e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.0e0

QD
type: SiteQuality
SIO_000300: 2.983e1

GenotypeQuality
all individuals: 3527
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2278
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2008
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2809
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3739
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12455
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3150
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3605
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7815
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523229246001523e-5
allele num: 65650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15200
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.103e0

MQ
type: SiteQuality
SIO_000300: 5.754e1

VQSLOD
type: SiteQuality
SIO_000300: -3.726e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQRankSum
type: SiteQuality
SIO_000300: -1.137e0

FS
type: SiteQuality
SIO_000300: 3.3432e1

QD
type: SiteQuality
SIO_000300: 2.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

DP
type: SiteQuality
SIO_000300: 1.707742e6

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 518
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55924
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.84e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

DP
type: SiteQuality
SIO_000300: 5.588432e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.49e-1

QD
type: SiteQuality
SIO_000300: 1.33e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.781e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55923
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 800
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.91e1

FS
type: SiteQuality
SIO_000300: 2.632e0

VQSLOD
type: SiteQuality
SIO_000300: -1.046e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

QD
type: SiteQuality
SIO_000300: 1.721e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.95e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.051e0

DP
type: SiteQuality
SIO_000300: 5.58848e6

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

GenotypeQuality
all individuals: 55923
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 585
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 921
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 518
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 752
bin: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

QD
type: SiteQuality
SIO_000300: 7.27e0

VQSLOD
type: SiteQuality
SIO_000300: -9.407e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.74e-1

DP
type: SiteQuality
SIO_000300: 5.588861e6

FS
type: SiteQuality
SIO_000300: 5.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 5.989e1

GenotypeQuality
all individuals: 55923
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 801
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 752
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 776
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 584
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 5.588689e6

VQSLOD
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 6.632e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.33e1

MQRankSum
type: SiteQuality
SIO_000300: -5.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.05e-1

GenotypeQuality
all individuals: 776
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 582
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 921
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55923
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 429
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.232e0

DP
type: SiteQuality
SIO_000300: 5.588668e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.221e1

MQ
type: SiteQuality
SIO_000300: 5.548e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.102e0

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.252e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.21e-1

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

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

GenotypeQuality
all individuals: 752
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 8.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.984e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.28e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

DP
type: SiteQuality
SIO_000300: 5.58858e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.74e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

QD
type: SiteQuality
SIO_000300: 1.323e1

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55923
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 800
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

FS
type: SiteQuality
SIO_000300: 1.429e0

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.372e1

DP
type: SiteQuality
SIO_000300: 5.588701e6