19-41787087-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787087
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787087
    reference: chr 19
allele count: 8
allele frequency: 6.590220113351786e-5
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469858
  ensembl transcript: ENST00000597725
  gene symbol: HNRNPUL1
  hgvsc: ENST00000597725.1:c.486T>C
  hgvsp: ENST00000597725.1:c.486T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.606T>C
  hgvsp: ENST00000595018.1:c.606T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2006T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.452T>C
  hgvsp: ENST00000599614.1:c.452T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.906T>C
  hgvsp: ENST00000392006.3:c.906T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.606T>C
  hgvsp: ENST00000599719.1:c.606T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.606T>C
  hgvsp: ENST00000593587.1:c.606T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.606T>C
  hgvsp: ENST00000352456.3:c.606T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4884T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.639T>C
  hgvsp: ENST00000263367.3:c.639T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*482T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.906T>C
  hgvsp: ENST00000602130.1:c.906T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12179
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr302Tyr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

19-41787096-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787096
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787096
    reference: chr 19
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.615A>G
  hgvsp: ENST00000593587.1:c.615A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4893A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.915A>G
  hgvsp: ENST00000392006.3:c.915A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.615A>G
  hgvsp: ENST00000595018.1:c.615A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.615A>G
  hgvsp: ENST00000352456.3:c.615A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.615A>G
  hgvsp: ENST00000599719.1:c.615A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469858
  ensembl transcript: ENST00000597725
  gene symbol: HNRNPUL1
  hgvsc: ENST00000597725.1:c.495A>G
  hgvsp: ENST00000597725.1:c.495A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*491A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.648A>G
  hgvsp: ENST00000263367.3:c.648A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2015A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.915A>G
  hgvsp: ENST00000602130.1:c.915A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.461A>G
  hgvsp: ENST00000599614.1:c.461A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12183
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly305Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-41787113-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787113
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787113
    reference: chr 19
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.665C>T
  hgvsp: ENSP00000263367.3:p.Ser222Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.632C>T
  hgvsp: ENSP00000473132.1:p.Ser211Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2032C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.932C>T
  hgvsp: ENSP00000470687.1:p.Ser311Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.632C>T
  hgvsp: ENSP00000470172.1:p.Ser211Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.632C>T
  hgvsp: ENSP00000472629.1:p.Ser211Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.632C>T
  hgvsp: ENSP00000340857.3:p.Ser211Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*508C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4910C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.932C>T
  hgvsp: ENSP00000375863.2:p.Ser311Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469858
  ensembl transcript: ENST00000597725
  gene symbol: HNRNPUL1
  hgvsc: ENST00000597725.1:c.512C>T
  hgvsp: ENSP00000469858.1:p.Ser171Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.478C>T
  hgvsp: ENSP00000473178.1:p.Ser160Phe
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser311Phe
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

19-41787115-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787115
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787115
    reference: chr 19
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4912A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.634A>G
  hgvsp: ENSP00000340857.3:p.Thr212Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.934A>G
  hgvsp: ENSP00000470687.1:p.Thr312Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2034A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.634A>G
  hgvsp: ENSP00000472629.1:p.Thr212Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469858
  ensembl transcript: ENST00000597725
  gene symbol: HNRNPUL1
  hgvsc: ENST00000597725.1:c.514A>G
  hgvsp: ENSP00000469858.1:p.Thr172Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.480A>G
  hgvsp: ENSP00000473178.1:p.Thr161Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.634A>G
  hgvsp: ENSP00000470172.1:p.Thr212Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.934A>G
  hgvsp: ENSP00000375863.2:p.Thr312Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.667A>G
  hgvsp: ENSP00000263367.3:p.Thr223Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.634A>G
  hgvsp: ENSP00000473132.1:p.Thr212Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*510A>G
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12176
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr312Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

19-41787119-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787119
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787119
    reference: chr 19
allele count: 21
allele frequency: 1.729932779754844e-4
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.671A>G
  hgvsp: ENSP00000263367.3:p.Asn224Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*514A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.638A>G
  hgvsp: ENSP00000472629.1:p.Asn213Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2038A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.938A>G
  hgvsp: ENSP00000375863.2:p.Asn313Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.638A>G
  hgvsp: ENSP00000473132.1:p.Asn213Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.484A>G
  hgvsp: ENSP00000473178.1:p.Asn162Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4916A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469858
  ensembl transcript: ENST00000597725
  gene symbol: HNRNPUL1
  hgvsc: ENST00000597725.1:c.518A>G
  hgvsp: ENST00000597725.1:c.518A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.638A>G
  hgvsp: ENSP00000340857.3:p.Asn213Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.638A>G
  hgvsp: ENSP00000470172.1:p.Asn213Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.938A>G
  hgvsp: ENSP00000470687.1:p.Asn313Ser
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12715
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Asn313Ser
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

19-41787120-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787120
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787120
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.639T>C
  hgvsp: ENST00000599719.1:c.639T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*515T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.672T>C
  hgvsp: ENST00000263367.3:c.672T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.939T>C
  hgvsp: ENST00000392006.3:c.939T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.639T>C
  hgvsp: ENST00000595018.1:c.639T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.485T>C
  hgvsp: ENST00000599614.1:c.485T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4917T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.939T>C
  hgvsp: ENST00000602130.1:c.939T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.639T>C
  hgvsp: ENST00000593587.1:c.639T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.639T>C
  hgvsp: ENST00000352456.3:c.639T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2039T>C
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn313Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum

19-41787124-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787124
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787124
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2043C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.643C>T
  hgvsp: ENSP00000473132.1:p.Arg215Trp
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.643C>T
  hgvsp: ENSP00000340857.3:p.Arg215Trp
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4921C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*519C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.676C>T
  hgvsp: ENSP00000263367.3:p.Arg226Trp
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.943C>T
  hgvsp: ENSP00000375863.2:p.Arg315Trp
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.643C>T
  hgvsp: ENSP00000472629.1:p.Arg215Trp
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.643C>T
  hgvsp: ENSP00000470172.1:p.Arg215Trp
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.943C>T
  hgvsp: ENSP00000470687.1:p.Arg315Trp
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.489C>T
  hgvsp: ENSP00000473178.1:p.Arg164Trp
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg315Trp
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP

19-41787125-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787125
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787125
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.644G>A
  hgvsp: ENSP00000472629.1:p.Arg215Gln
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*520G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.644G>A
  hgvsp: ENSP00000473132.1:p.Arg215Gln
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.644G>A
  hgvsp: ENSP00000340857.3:p.Arg215Gln
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.644G>A
  hgvsp: ENSP00000470172.1:p.Arg215Gln
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.944G>A
  hgvsp: ENSP00000375863.2:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.677G>A
  hgvsp: ENSP00000263367.3:p.Arg226Gln
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.490G>A
  hgvsp: ENSP00000473178.1:p.Arg164Gln
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4922G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2044G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.944G>A
  hgvsp: ENSP00000470687.1:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31119
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg315Gln
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

19-41787132-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787132
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787132
    reference: chr 19
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2051A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.684A>G
  hgvsp: ENST00000263367.3:c.684A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.951A>G
  hgvsp: ENST00000392006.3:c.951A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.651A>G
  hgvsp: ENST00000352456.3:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.497A>G
  hgvsp: ENST00000599614.1:c.497A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4929A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.951A>G
  hgvsp: ENST00000602130.1:c.951A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.651A>G
  hgvsp: ENST00000595018.1:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*527A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.651A>G
  hgvsp: ENST00000593587.1:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.651A>G
  hgvsp: ENST00000599719.1:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31119
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu317Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/19-41787143-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787143
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787143
    reference: chr 19
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*538A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.662A>C
  hgvsp: ENSP00000472629.1:p.Asp221Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.508A>C
  hgvsp: ENSP00000473178.1:p.Asp170Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.662A>C
  hgvsp: ENSP00000340857.3:p.Asp221Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.695A>C
  hgvsp: ENSP00000263367.3:p.Asp232Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4940A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2062A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.962A>C
  hgvsp: ENSP00000375863.2:p.Asp321Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.962A>C
  hgvsp: ENSP00000470687.1:p.Asp321Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.662A>C
  hgvsp: ENSP00000473132.1:p.Asp221Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.662A>C
  hgvsp: ENSP00000470172.1:p.Asp221Ala
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp321Ala
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: A
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-41787145-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787145
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787145
    reference: chr 19
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.964A>G
  hgvsp: ENSP00000375863.2:p.Lys322Glu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4942A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.697A>G
  hgvsp: ENSP00000263367.3:p.Lys233Glu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.664A>G
  hgvsp: ENSP00000472629.1:p.Lys222Glu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.664A>G
  hgvsp: ENSP00000473132.1:p.Lys222Glu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.664A>G
  hgvsp: ENSP00000340857.3:p.Lys222Glu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.964A>G
  hgvsp: ENSP00000470687.1:p.Lys322Glu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.664A>G
  hgvsp: ENSP00000470172.1:p.Lys222Glu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2064A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.510A>G
  hgvsp: ENSP00000473178.1:p.Lys171Glu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*540A>G
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys322Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

19-41787159-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787159
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787159
    reference: chr 19
allele count: 6
allele frequency: 4.946984812756625e-5
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2078C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.678C>T
  hgvsp: ENST00000593587.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4956C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.678C>T
  hgvsp: ENST00000595018.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.678C>T
  hgvsp: ENST00000599719.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.978C>T
  hgvsp: ENST00000602130.1:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.978C>T
  hgvsp: ENST00000392006.3:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.678C>T
  hgvsp: ENST00000352456.3:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*554C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.711C>T
  hgvsp: ENST00000263367.3:c.711C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.524C>T
  hgvsp: ENST00000599614.1:c.524C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn326Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

19-41787168-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787168
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787168
    reference: chr 19
allele count: 3
allele frequency: 2.478191911181602e-5
allele num: 121056
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.987T>A
  hgvsp: ENST00000602130.1:c.987T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.987T>A
  hgvsp: ENST00000392006.3:c.987T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.687T>A
  hgvsp: ENST00000352456.3:c.687T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4965T>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.687T>A
  hgvsp: ENST00000595018.1:c.687T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.687T>A
  hgvsp: ENST00000593587.1:c.687T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2087T>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.533T>A
  hgvsp: ENST00000599614.1:c.533T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*563T>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.687T>A
  hgvsp: ENST00000599719.1:c.687T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.720T>A
  hgvsp: ENST00000263367.3:c.720T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile329Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

19-41787179-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787179
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787179
    reference: chr 19
allele count: 1
allele frequency: 8.29393713195654e-6
allele num: 120570
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.698C>T
  hgvsp: ENSP00000472629.1:p.Ala233Val
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.731C>T
  hgvsp: ENSP00000263367.3:p.Ala244Val
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2098C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.544C>T
  hgvsp: ENSP00000473178.1:p.Ala182Val
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.698C>T
  hgvsp: ENSP00000340857.3:p.Ala233Val
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.698C>T
  hgvsp: ENSP00000470172.1:p.Ala233Val
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.998C>T
  hgvsp: ENSP00000470687.1:p.Ala333Val
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*574C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4976C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.698C>T
  hgvsp: ENSP00000473132.1:p.Ala233Val
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.998C>T
  hgvsp: ENSP00000375863.2:p.Ala333Val
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala333Val
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

19-41787193-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787193
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787193
    reference: chr 19
allele count: 2
allele frequency: 1.682538614261197e-5
allele num: 118868
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.732+13A>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.545+13A>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.699+13A>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.999+13A>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.699+13A>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*575+13A>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.699+13A>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4990A>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.699+13A>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2112A>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.999+13A>T
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27827
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6614
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

19-41787197-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787197
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787197
    reference: chr 19
allele count: 2
allele frequency: 1.690874351126968e-5
allele num: 118282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.699+17T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2116T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4994T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*575+17T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.699+17T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.699+17T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.999+17T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.699+17T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.732+17T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.999+17T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.545+17T>G
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26654
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10147
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1739
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

19-41787198-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787198
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787198
    reference: chr 19
allele count: 1
allele frequency: 8.463100880162492e-6
allele num: 118160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.699+18G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.699+18G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.699+18G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*575+18G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.999+18G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.545+18G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.999+18G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.732+18G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+4995G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2117G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.699+18G>A
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26332
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1205
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum

19-41787208-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787208
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787208
    reference: chr 19
allele count: 1
allele frequency: 8.558859275235797e-6
allele num: 116838
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.999+28G>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.699+28G>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+5005G>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.999+28G>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*575+28G>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.699+28G>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.545+28G>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2127G>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.732+28G>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.699+28G>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.699+28G>T
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1854
  bin: 9.75e1
  variant carriers: 1
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: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

19-41787220-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787220
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787220
    reference: chr 19
allele count: 2
allele frequency: 1.745352997643774e-5
allele num: 114590
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.699+40G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.699+40G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2139G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.732+40G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.545+40G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.699+40G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+5017G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.699+40G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.999+40G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*575+40G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.999+40G>A
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12766
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

19-41787221-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787221
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787221
    reference: chr 19
allele count: 2
allele frequency: 1.751620248730075e-5
allele num: 114180
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.699+41T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.732+41T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+5018T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.699+41T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.999+41T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2140T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.699+41T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.699+41T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.999+41T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.545+41T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*575+41T>C
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

19-41787228-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787228
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787228
    reference: chr 19
allele count: 1
allele frequency: 9.015019021690137e-6
allele num: 110926
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.999+48A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2147A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*575+48A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.699+48A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.732+48A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.545+48A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.999+48A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+5025A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.699+48A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.699+48A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.699+48A>G
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10755
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13787
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16841
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8152
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/19-41787230-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41787230
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41787230
    reference: chr 19
allele count: 1
allele frequency: 9.11244760342628e-6
allele num: 109740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.657+5027A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.999+50A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.699+50A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.732+50A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.699+50A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.545+50A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.699+50A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.263+2149A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.999+50A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.699+50A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*575+50A>C
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11563
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16726
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

19-41798101-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798101
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798101
    reference: chr 19
allele count: 2
allele frequency: 1.68214237653075e-5
allele num: 118896
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.700-49T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.264-49T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.658-49T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1000-49T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.733-49T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.700-49T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1000-49T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.700-49T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.546-49T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*576-49T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.700-49T>C
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12983
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

19-41798106-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798106
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798106
    reference: chr 19
allele count: 274
allele frequency: 2.30321778016879e-3
allele num: 118964
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.546-44A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.264-44A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1000-44A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.700-44A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*576-44A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.733-44A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.700-44A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1000-44A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.658-44A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.700-44A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.700-44A>G
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5813
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13003
  bin: 9.75e1
  variant carriers: 189
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4724
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum

19-41798107-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798107
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798107
    reference: chr 19
allele count: 1
allele frequency: 8.407741848694278e-6
allele num: 118938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.546-43T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.658-43T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1000-43T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.700-43T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.700-43T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.700-43T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.733-43T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.264-43T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*576-43T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1000-43T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.700-43T>C
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12865
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5833
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

19-41798110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798110
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798110
    reference: chr 19
allele count: 7
allele frequency: 5.88621112998436e-5
allele num: 118922
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.264-40C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.658-40C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.700-40C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.700-40C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1000-40C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.733-40C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.546-40C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.700-40C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1000-40C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*576-40C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.700-40C>T
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4094
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5833
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12867
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1066
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP

19-41798111-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798111
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798111
    reference: chr 19
allele count: 21759
allele frequency: 1.820288448668184e-1
allele num: 119536
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1000-39A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.700-39A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.264-39A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.658-39A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.733-39A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*576-39A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.546-39A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.700-39A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.700-39A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1000-39A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.700-39A>G
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15369
  bin: 9.75e1
  variant carriers: 14913
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 7.25e1
  variant carriers: 239
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 6.25e1
  variant carriers: 194
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 3.75e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 2.25e1
  variant carriers: 421
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 5.75e1
  variant carriers: 185
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.75e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 2.75e1
  variant carriers: 247
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 1.75e1
  variant carriers: 575
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 7.5e0
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 8.75e1
  variant carriers: 413
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 8.25e1
  variant carriers: 317
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 1.25e1
  variant carriers: 390
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 5.25e1
  variant carriers: 157
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 7.75e1
  variant carriers: 299
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.25e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 6.75e1
  variant carriers: 208
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 432
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 3.25e1
  variant carriers: 167
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 3.75e1
  variant carriers: 22
num of homozygotes: 2251
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

19-41798112-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798112
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798112
    reference: chr 19
allele count: 1
allele frequency: 8.361064196250898e-6
allele num: 119602
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.658-38A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1000-38A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.700-38A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.546-38A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.700-38A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1000-38A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.700-38A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.733-38A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.264-38A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.700-38A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*576-38A>G
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

19-41798121-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798121
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798121
    reference: chr 19
allele count: 1
allele frequency: 8.338475393159114e-6
allele num: 119926
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.700-29A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.700-29A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*576-29A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.546-29A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.733-29A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1000-29A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.264-29A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.658-29A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.700-29A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.700-29A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1000-29A>G
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5133
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

19-41798123-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798123
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798123
    reference: chr 19
allele count: 3
allele frequency: 2.499958334027766e-5
allele num: 120002
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.264-27T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*576-27T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.700-27T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.733-27T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.700-27T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.658-27T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1000-27T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.546-27T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.700-27T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1000-27T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.700-27T>C
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
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: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

19-41798125-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798125
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798125
    reference: chr 19
allele count: 1
allele frequency: 8.323068215867098e-6
allele num: 120148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.700-25A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.658-25A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1000-25A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.733-25A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*576-25A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.264-25A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.700-25A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.700-25A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.700-25A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.546-25A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1000-25A>G
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

19-41798130-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798130
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798130
    reference: chr 19
allele count: 1
allele frequency: 8.306199747491528e-6
allele num: 120392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.658-20C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1000-20C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.264-20C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.546-20C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.733-20C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1000-20C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.700-20C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.700-20C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*576-20C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.700-20C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.700-20C>T
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3100
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

19-41798171-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798171
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798171
    reference: chr 19
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*597G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1021G>A
  hgvsp: ENSP00000470687.1:p.Val341Met
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.721G>A
  hgvsp: ENSP00000472629.1:p.Val241Met
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.754G>A
  hgvsp: ENSP00000263367.3:p.Val252Met
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.679G>A
  hgvsp: ENSP00000367460.3:p.Val227Met
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.721G>A
  hgvsp: ENSP00000340857.3:p.Val241Met
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1021G>A
  hgvsp: ENSP00000375863.2:p.Val341Met
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.567G>A
  hgvsp: ENSP00000473178.1:p.Val190Met
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*14G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.721G>A
  hgvsp: ENSP00000470172.1:p.Val241Met
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.721G>A
  hgvsp: ENSP00000473132.1:p.Val241Met
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val341Met
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

19-41798186-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798186
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798186
    reference: chr 19
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.736A>G
  hgvsp: ENSP00000340857.3:p.Thr246Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.769A>G
  hgvsp: ENSP00000263367.3:p.Thr257Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.736A>G
  hgvsp: ENSP00000472629.1:p.Thr246Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.582A>G
  hgvsp: ENSP00000473178.1:p.Thr195Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*29A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1036A>G
  hgvsp: ENSP00000375863.2:p.Thr346Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.736A>G
  hgvsp: ENSP00000470172.1:p.Thr246Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*612A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1036A>G
  hgvsp: ENSP00000470687.1:p.Thr346Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.694A>G
  hgvsp: ENSP00000367460.3:p.Thr232Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.736A>G
  hgvsp: ENSP00000473132.1:p.Thr246Ala
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr346Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD

19-41798201-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798201
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798201
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*627T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.709T>C
  hgvsp: ENSP00000367460.3:p.Trp237Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.751T>C
  hgvsp: ENSP00000470172.1:p.Trp251Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.751T>C
  hgvsp: ENSP00000473132.1:p.Trp251Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.751T>C
  hgvsp: ENSP00000472629.1:p.Trp251Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.751T>C
  hgvsp: ENSP00000340857.3:p.Trp251Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*44T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1051T>C
  hgvsp: ENSP00000470687.1:p.Trp351Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.784T>C
  hgvsp: ENSP00000263367.3:p.Trp262Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.597T>C
  hgvsp: ENSP00000473178.1:p.Trp200Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1051T>C
  hgvsp: ENSP00000375863.2:p.Trp351Arg
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp351Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS

http://identifiers.org/exac.variant/19-41798222-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798222
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798222
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.805A>C
  hgvsp: ENSP00000263367.3:p.Ile269Leu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.772A>C
  hgvsp: ENSP00000470172.1:p.Ile258Leu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1072A>C
  hgvsp: ENSP00000375863.2:p.Ile358Leu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.772A>C
  hgvsp: ENSP00000340857.3:p.Ile258Leu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.618A>C
  hgvsp: ENSP00000473178.1:p.Ile207Leu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.730A>C
  hgvsp: ENSP00000367460.3:p.Ile244Leu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.772A>C
  hgvsp: ENSP00000473132.1:p.Ile258Leu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.772A>C
  hgvsp: ENSP00000472629.1:p.Ile258Leu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1072A>C
  hgvsp: ENSP00000470687.1:p.Ile358Leu
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*648A>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*65A>C
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 3.75e1
  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: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile358Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD

19-41798239-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798239
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798239
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.789G>C
  hgvsp: ENSP00000472629.1:p.Leu263Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.789G>C
  hgvsp: ENSP00000473132.1:p.Leu263Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1089G>C
  hgvsp: ENSP00000470687.1:p.Leu363Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.635G>C
  hgvsp: ENSP00000473178.1:p.Leu212Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*82G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.789G>C
  hgvsp: ENSP00000470172.1:p.Leu263Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.747G>C
  hgvsp: ENSP00000367460.3:p.Leu249Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.822G>C
  hgvsp: ENSP00000263367.3:p.Leu274Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*665G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.789G>C
  hgvsp: ENSP00000340857.3:p.Leu263Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1089G>C
  hgvsp: ENSP00000375863.2:p.Leu363Phe
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 4.25e1
  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: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu363Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

19-41798239-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798239
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798239
    reference: chr 19
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.822G>T
  hgvsp: ENSP00000263367.3:p.Leu274Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.789G>T
  hgvsp: ENSP00000340857.3:p.Leu263Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.789G>T
  hgvsp: ENSP00000473132.1:p.Leu263Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.789G>T
  hgvsp: ENSP00000472629.1:p.Leu263Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1089G>T
  hgvsp: ENSP00000470687.1:p.Leu363Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*82G>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.789G>T
  hgvsp: ENSP00000470172.1:p.Leu263Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1089G>T
  hgvsp: ENSP00000375863.2:p.Leu363Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.635G>T
  hgvsp: ENSP00000473178.1:p.Leu212Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.747G>T
  hgvsp: ENSP00000367460.3:p.Leu249Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*665G>T
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu363Phe
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

19-41798243-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798243
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798243
    reference: chr 19
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.793G>C
  hgvsp: ENSP00000472629.1:p.Gly265Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.793G>C
  hgvsp: ENSP00000470172.1:p.Gly265Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*86G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.793G>C
  hgvsp: ENSP00000340857.3:p.Gly265Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.826G>C
  hgvsp: ENSP00000263367.3:p.Gly276Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.793G>C
  hgvsp: ENSP00000473132.1:p.Gly265Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.751G>C
  hgvsp: ENSP00000367460.3:p.Gly251Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1093G>C
  hgvsp: ENSP00000375863.2:p.Gly365Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*669G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.639G>C
  hgvsp: ENSP00000473178.1:p.Gly214Arg
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1093G>C
  hgvsp: ENSP00000470687.1:p.Gly365Arg
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7123
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly365Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

19-41798252-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798252
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798252
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.802C>T
  hgvsp: ENSP00000340857.3:p.Leu268Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1102C>T
  hgvsp: ENSP00000375863.2:p.Leu368Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.648C>T
  hgvsp: ENSP00000473178.1:p.Leu217Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.802C>T
  hgvsp: ENSP00000472629.1:p.Leu268Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.835C>T
  hgvsp: ENSP00000263367.3:p.Leu279Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*95C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.802C>T
  hgvsp: ENSP00000470172.1:p.Leu268Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.802C>T
  hgvsp: ENSP00000473132.1:p.Leu268Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.760C>T
  hgvsp: ENSP00000367460.3:p.Leu254Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1102C>T
  hgvsp: ENSP00000470687.1:p.Leu368Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*678C>T
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu368Phe
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

19-41798278-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798278
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798278
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.828T>C
  hgvsp: ENST00000595018.1:c.828T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*704T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*121T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.861T>C
  hgvsp: ENST00000263367.3:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.828T>C
  hgvsp: ENST00000593587.1:c.828T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.828T>C
  hgvsp: ENST00000352456.3:c.828T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.674T>C
  hgvsp: ENST00000599614.1:c.674T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.786T>C
  hgvsp: ENST00000378215.4:c.786T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1128T>C
  hgvsp: ENST00000392006.3:c.1128T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1128T>C
  hgvsp: ENST00000602130.1:c.1128T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.828T>C
  hgvsp: ENST00000599719.1:c.828T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn376Asn
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

19-41798281-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798281
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798281
    reference: chr 19
allele count: 7
allele frequency: 5.765682656826568e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.789C>T
  hgvsp: ENST00000378215.4:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*707C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.831C>T
  hgvsp: ENST00000593587.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.864C>T
  hgvsp: ENST00000263367.3:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1131C>T
  hgvsp: ENST00000602130.1:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.677C>T
  hgvsp: ENST00000599614.1:c.677C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.831C>T
  hgvsp: ENST00000352456.3:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.831C>T
  hgvsp: ENST00000595018.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.831C>T
  hgvsp: ENST00000599719.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*124C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1131C>T
  hgvsp: ENST00000392006.3:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Cys377Cys
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

19-41798290-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798290
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798290
    reference: chr 19
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.840G>A
  hgvsp: ENST00000595018.1:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.686G>A
  hgvsp: ENST00000599614.1:c.686G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.873G>A
  hgvsp: ENST00000263367.3:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.840G>A
  hgvsp: ENST00000352456.3:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.798G>A
  hgvsp: ENST00000378215.4:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*133G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1140G>A
  hgvsp: ENST00000602130.1:c.1140G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.840G>A
  hgvsp: ENST00000593587.1:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1140G>A
  hgvsp: ENST00000392006.3:c.1140G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*716G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.840G>A
  hgvsp: ENST00000599719.1:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7145
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu380Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

19-41798299-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798299
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798299
    reference: chr 19
allele count: 4
allele frequency: 3.29489291598023e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.882C>T
  hgvsp: ENST00000263367.3:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.807C>T
  hgvsp: ENST00000378215.4:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.695C>T
  hgvsp: ENST00000599614.1:c.695C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.849C>T
  hgvsp: ENST00000593587.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1149C>T
  hgvsp: ENST00000392006.3:c.1149C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1149C>T
  hgvsp: ENST00000602130.1:c.1149C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.849C>T
  hgvsp: ENST00000352456.3:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.849C>T
  hgvsp: ENST00000595018.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*725C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.849C>T
  hgvsp: ENST00000599719.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*142C>T
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7145
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe383Phe
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ

19-41798314-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798314
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798314
    reference: chr 19
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.897G>A
  hgvsp: ENST00000263367.3:c.897G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.864G>A
  hgvsp: ENST00000352456.3:c.864G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.710G>A
  hgvsp: ENST00000599614.1:c.710G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1164G>A
  hgvsp: ENST00000392006.3:c.1164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.864G>A
  hgvsp: ENST00000599719.1:c.864G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.864G>A
  hgvsp: ENST00000593587.1:c.864G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.822G>A
  hgvsp: ENST00000378215.4:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*740G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*157G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.864G>A
  hgvsp: ENST00000595018.1:c.864G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1164G>A
  hgvsp: ENST00000602130.1:c.1164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu388Glu
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

19-41798315-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798315
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798315
    reference: chr 19
allele count: 17
allele frequency: 1.40069870146991e-4
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.865C>T
  hgvsp: ENSP00000340857.3:p.Pro289Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.865C>T
  hgvsp: ENSP00000473132.1:p.Pro289Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.898C>T
  hgvsp: ENSP00000263367.3:p.Pro300Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1165C>T
  hgvsp: ENSP00000375863.2:p.Pro389Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.823C>T
  hgvsp: ENSP00000367460.3:p.Pro275Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.865C>T
  hgvsp: ENSP00000472629.1:p.Pro289Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.711C>T
  hgvsp: ENSP00000473178.1:p.Pro238Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.865C>T
  hgvsp: ENSP00000470172.1:p.Pro289Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1165C>T
  hgvsp: ENSP00000470687.1:p.Pro389Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*158C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*741C>T
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro389Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

19-41798319-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798319
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798319
    reference: chr 19
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1169A>G
  hgvsp: ENSP00000375863.2:p.Tyr390Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.827A>G
  hgvsp: ENSP00000367460.3:p.Tyr276Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.869A>G
  hgvsp: ENSP00000473132.1:p.Tyr290Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.715A>G
  hgvsp: ENSP00000473178.1:p.Tyr239Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*162A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.869A>G
  hgvsp: ENSP00000340857.3:p.Tyr290Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.902A>G
  hgvsp: ENSP00000263367.3:p.Tyr301Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.869A>G
  hgvsp: ENSP00000472629.1:p.Tyr290Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1169A>G
  hgvsp: ENSP00000470687.1:p.Tyr390Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.869A>G
  hgvsp: ENSP00000470172.1:p.Tyr290Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*745A>G
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr390Cys
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

19-41798322-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798322
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798322
    reference: chr 19
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.830G>C
  hgvsp: ENSP00000367460.3:p.Cys277Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.872G>C
  hgvsp: ENSP00000340857.3:p.Cys291Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.905G>C
  hgvsp: ENSP00000263367.3:p.Cys302Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1172G>C
  hgvsp: ENSP00000375863.2:p.Cys391Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.872G>C
  hgvsp: ENSP00000470172.1:p.Cys291Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.718G>C
  hgvsp: ENSP00000473178.1:p.Cys240Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.872G>C
  hgvsp: ENSP00000472629.1:p.Cys291Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.872G>C
  hgvsp: ENSP00000473132.1:p.Cys291Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1172G>C
  hgvsp: ENSP00000470687.1:p.Cys391Ser
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*748G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*165G>C
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys391Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

19-41798330-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798330
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798330
    reference: chr 19
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*173C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.880C>T
  hgvsp: ENSP00000472629.1:p.Leu294Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.880C>T
  hgvsp: ENSP00000340857.3:p.Leu294Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.880C>T
  hgvsp: ENSP00000473132.1:p.Leu294Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.838C>T
  hgvsp: ENSP00000367460.3:p.Leu280Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1180C>T
  hgvsp: ENSP00000470687.1:p.Leu394Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.880C>T
  hgvsp: ENSP00000470172.1:p.Leu294Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.913C>T
  hgvsp: ENSP00000263367.3:p.Leu305Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*756C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.726C>T
  hgvsp: ENSP00000473178.1:p.Leu243Phe
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1180C>T
  hgvsp: ENSP00000375863.2:p.Leu394Phe
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu394Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

19-41798338-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798338
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798338
    reference: chr 19
allele count: 2
allele frequency: 1.650028875505322e-5
allele num: 121210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.734G>T
  hgvsp: ENST00000599614.1:c.734G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.888G>T
  hgvsp: ENST00000593587.1:c.888G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*764G>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1188G>T
  hgvsp: ENST00000392006.3:c.1188G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.921G>T
  hgvsp: ENST00000263367.3:c.921G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.846G>T
  hgvsp: ENST00000378215.4:c.846G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*181G>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.888G>T
  hgvsp: ENST00000595018.1:c.888G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1188G>T
  hgvsp: ENST00000602130.1:c.1188G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.888G>T
  hgvsp: ENST00000599719.1:c.888G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.888G>T
  hgvsp: ENST00000352456.3:c.888G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly396Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

19-41798360-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798360
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798360
    reference: chr 19
allele count: 2
allele frequency: 1.653439153439154e-5
allele num: 120960
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*203C>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.756C>G
  hgvsp: ENSP00000473178.1:p.Pro253Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*786C>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.910C>G
  hgvsp: ENSP00000473132.1:p.Pro304Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.910C>G
  hgvsp: ENSP00000340857.3:p.Pro304Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.910C>G
  hgvsp: ENSP00000470172.1:p.Pro304Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1210C>G
  hgvsp: ENSP00000375863.2:p.Pro404Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.910C>G
  hgvsp: ENSP00000472629.1:p.Pro304Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.943C>G
  hgvsp: ENSP00000263367.3:p.Pro315Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.868C>G
  hgvsp: ENSP00000367460.3:p.Pro290Ala
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1210C>G
  hgvsp: ENSP00000470687.1:p.Pro404Ala
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro404Ala
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

19-41798372-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798372
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798372
    reference: chr 19
allele count: 1
allele frequency: 8.279927799029592e-6
allele num: 120774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.880C>T
  hgvsp: ENSP00000367460.3:p.Arg294Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*215C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.768C>T
  hgvsp: ENSP00000473178.1:p.Arg257Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.955C>T
  hgvsp: ENSP00000263367.3:p.Arg319Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.922C>T
  hgvsp: ENSP00000470172.1:p.Arg308Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.922C>T
  hgvsp: ENSP00000340857.3:p.Arg308Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1222C>T
  hgvsp: ENSP00000375863.2:p.Arg408Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1222C>T
  hgvsp: ENSP00000470687.1:p.Arg408Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.922C>T
  hgvsp: ENSP00000473132.1:p.Arg308Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.922C>T
  hgvsp: ENSP00000472629.1:p.Arg308Cys
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*798C>T
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg408Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

19-41798376-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798376
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798376
    reference: chr 19
allele count: 9
allele frequency: 7.453416149068323e-5
allele num: 120750
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1226T>C
  hgvsp: ENSP00000470687.1:p.Ile409Thr
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*219T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.926T>C
  hgvsp: ENSP00000340857.3:p.Ile309Thr
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.926T>C
  hgvsp: ENSP00000473132.1:p.Ile309Thr
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.926T>C
  hgvsp: ENSP00000472629.1:p.Ile309Thr
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.884T>C
  hgvsp: ENSP00000367460.3:p.Ile295Thr
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.772T>C
  hgvsp: ENSP00000473178.1:p.Ile258Thr
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.959T>C
  hgvsp: ENSP00000263367.3:p.Ile320Thr
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1226T>C
  hgvsp: ENSP00000375863.2:p.Ile409Thr
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.926T>C
  hgvsp: ENSP00000470172.1:p.Ile309Thr
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*802T>C
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile409Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/19-41798378-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798378
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798378
    reference: chr 19
allele count: 2
allele frequency: 1.656561640658649e-5
allele num: 120732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.774C>A
  hgvsp: ENST00000599614.1:c.774C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1228C>A
  hgvsp: ENST00000392006.3:c.1228C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.928C>A
  hgvsp: ENST00000593587.1:c.928C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.961C>A
  hgvsp: ENST00000263367.3:c.961C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.928C>A
  hgvsp: ENST00000352456.3:c.928C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.928C>A
  hgvsp: ENST00000599719.1:c.928C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*221C>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.928C>A
  hgvsp: ENST00000595018.1:c.928C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.886C>A
  hgvsp: ENST00000378215.4:c.886C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*804C>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1228C>A
  hgvsp: ENST00000602130.1:c.1228C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg410Arg
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD

19-41798386-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798386
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798386
    reference: chr 19
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.894C>T
  hgvsp: ENST00000378215.4:c.894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.936C>T
  hgvsp: ENST00000593587.1:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1236C>T
  hgvsp: ENST00000602130.1:c.1236C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.969C>T
  hgvsp: ENST00000263367.3:c.969C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*812C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1236C>T
  hgvsp: ENST00000392006.3:c.1236C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.936C>T
  hgvsp: ENST00000352456.3:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*229C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.782C>T
  hgvsp: ENST00000599614.1:c.782C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.936C>T
  hgvsp: ENST00000599719.1:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.936C>T
  hgvsp: ENST00000595018.1:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr412Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

19-41798387-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798387
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798387
    reference: chr 19
allele count: 2
allele frequency: 1.658072325114821e-5
allele num: 120622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.937G>A
  hgvsp: ENSP00000470172.1:p.Val313Ile
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*813G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.783G>A
  hgvsp: ENSP00000473178.1:p.Val262Ile
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.937G>A
  hgvsp: ENSP00000473132.1:p.Val313Ile
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.937G>A
  hgvsp: ENSP00000340857.3:p.Val313Ile
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.895G>A
  hgvsp: ENSP00000367460.3:p.Val299Ile
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.937G>A
  hgvsp: ENSP00000472629.1:p.Val313Ile
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1237G>A
  hgvsp: ENSP00000470687.1:p.Val413Ile
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*230G>A
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.970G>A
  hgvsp: ENSP00000263367.3:p.Val324Ile
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1237G>A
  hgvsp: ENSP00000375863.2:p.Val413Ile
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val413Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

19-41798392-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798392
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798392
    reference: chr 19
allele count: 31
allele frequency: 2.57150441303338e-4
allele num: 120552
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1242A>G
  hgvsp: ENST00000392006.3:c.1242A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.942A>G
  hgvsp: ENST00000595018.1:c.942A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.900A>G
  hgvsp: ENST00000378215.4:c.900A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.942A>G
  hgvsp: ENST00000593587.1:c.942A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.788A>G
  hgvsp: ENST00000599614.1:c.788A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.975A>G
  hgvsp: ENST00000263367.3:c.975A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*235A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.942A>G
  hgvsp: ENST00000352456.3:c.942A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.942A>G
  hgvsp: ENST00000599719.1:c.942A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*818A>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1242A>G
  hgvsp: ENST00000602130.1:c.1242A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Gly414Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

19-41798423-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798423
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798423
    reference: chr 19
allele count: 2
allele frequency: 1.663865825859803e-5
allele num: 120202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.812+7G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.966+7G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*842+7G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1266+7G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*259+7G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.924+7G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.966+7G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.999+7G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.966+7G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1266+7G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.966+7G>C
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7118
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1266+7G>C
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

19-41798430-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798430
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798430
    reference: chr 19
allele count: 1
allele frequency: 8.326671995736744e-6
allele num: 120096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*259+14G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.966+14G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.966+14G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.999+14G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1266+14G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.924+14G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.966+14G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.812+14G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.966+14G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*842+14G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1266+14G>C
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  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: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

19-41798437-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798437
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798437
    reference: chr 19
allele count: 2
allele frequency: 1.666361167119361e-5
allele num: 120022
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.999+21T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.966+21T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.924+21T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*842+21T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1266+21T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.812+21T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.966+21T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.966+21T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.966+21T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1266+21T>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*259+21T>C
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

19-41798438-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798438
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798438
    reference: chr 19
allele count: 1
allele frequency: 8.331805835596807e-6
allele num: 120022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.966+22T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*842+22T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1266+22T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*259+22T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.924+22T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.966+22T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.966+22T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.999+22T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.812+22T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1266+22T>G
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.966+22T>G
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-41798441-T-TGGCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798441
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798445
    reference: chr 19
allele count: 1
allele frequency: 8.336807002917883e-6
allele num: 119950
alternate allele: TGGCC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1266+26_1266+29dupGGCC
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*842+26_*842+29dupGGCC
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.924+26_924+29dupGGCC
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.966+26_966+29dupGGCC
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.999+26_999+29dupGGCC
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.966+26_966+29dupGGCC
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.812+26_812+29dupGGCC
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.966+26_966+29dupGGCC
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1266+26_1266+29dupGGCC
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.966+26_966+29dupGGCC
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*259+26_*259+29dupGGCC
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

19-41798444-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798444
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798444
    reference: chr 19
allele count: 1
allele frequency: 8.34153584357952e-6
allele num: 119882
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.966+28C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.999+28C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.966+28C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.924+28C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*842+28C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.966+28C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.966+28C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*259+28C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1266+28C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1266+28C>T
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.812+28C>T
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

19-41798461-CAGAGG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798461
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798456
    reference: chr 19
allele count: 1
allele frequency: 8.424174009738345e-6
allele num: 118706
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1266+49_1266+53delGGAGA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.966+49_966+53delGGAGA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.924+49_924+53delGGAGA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.966+49_966+53delGGAGA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.966+49_966+53delGGAGA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*259+49_*259+53delGGAGA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.812+49_812+53delGGAGA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1266+49_1266+53delGGAGA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.999+49_999+53delGGAGA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.966+49_966+53delGGAGA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*842+49_*842+53delGGAGA
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7908
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6113
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: CAGAGG
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

19-41798466-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798466
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798466
    reference: chr 19
allele count: 1
allele frequency: 8.580597552813579e-6
allele num: 116542
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*842+50G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.999+50G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.966+50G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.924+50G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1266+50G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.966+50G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.966+50G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.812+50G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1266+50G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*259+50G>C
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.966+50G>C
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6680
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7648
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

19-41798468-G-GAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798468
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798470
    reference: chr 19
allele count: 1552
allele frequency: 1.5016351568396e-2
allele num: 103354
alternate allele: GAC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1266+74_1266+75dupCA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*842+74_*842+75dupCA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*259+74_*259+75dupCA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.999+74_999+75dupCA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.812+74_812+75dupCA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.966+74_966+75dupCA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.924+74_924+75dupCA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.966+74_966+75dupCA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.966+74_966+75dupCA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1266+74_1266+75dupCA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.966+74_966+75dupCA
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 1.75e1
  variant carriers: 163
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 4.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 3.75e1
  variant carriers: 198
genotype depth: GenotypeDepth
  all individuals: 10662
  bin: 3.25e1
  variant carriers: 278
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 5.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 1.25e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10857
  bin: 2.75e1
  variant carriers: 313
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 7.5e0
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 4.25e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8395
  bin: 2.25e1
  variant carriers: 256
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 5.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 4.75e1
  variant carriers: 10
num of homozygotes: 1
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

19-41798468-G-GACAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798468
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798472
    reference: chr 19
allele count: 36
allele frequency: 3.483174332875361e-4
allele num: 103354
alternate allele: GACAC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1266+72_1266+75dupCACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.966+72_966+75dupCACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*259+72_*259+75dupCACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.812+72_812+75dupCACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1266+72_1266+75dupCACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.999+72_999+75dupCACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.966+72_966+75dupCACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.924+72_924+75dupCACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*842+72_*842+75dupCACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.966+72_966+75dupCACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.966+72_966+75dupCACA
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10857
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 8395
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10662
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

19-41798468-G-GACACAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 41798468
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 41798474
    reference: chr 19
allele count: 227
allele frequency: 2.196334926563074e-3
allele num: 103354
alternate allele: GACACAC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000469934
  ensembl transcript: ENST00000600596
  gene symbol: HNRNPUL1
  hgvsc: ENST00000600596.1:c.*259+70_*259+75dupCACACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472629
  ensembl transcript: ENST00000593587
  gene symbol: HNRNPUL1
  hgvsc: ENST00000593587.1:c.966+70_966+75dupCACACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000375863
  ensembl transcript: ENST00000392006
  gene symbol: HNRNPUL1
  hgvsc: ENST00000392006.3:c.1266+70_1266+75dupCACACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473178
  ensembl transcript: ENST00000599614
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599614.1:c.812+70_812+75dupCACACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000340857
  ensembl transcript: ENST00000352456
  gene symbol: HNRNPUL1
  hgvsc: ENST00000352456.3:c.966+70_966+75dupCACACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000263367
  ensembl transcript: ENST00000263367
  gene symbol: HNRNPUL1
  hgvsc: ENST00000263367.3:c.999+70_999+75dupCACACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000473132
  ensembl transcript: ENST00000595018
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595018.1:c.966+70_966+75dupCACACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470172
  ensembl transcript: ENST00000599719
  gene symbol: HNRNPUL1
  hgvsc: ENST00000599719.1:c.966+70_966+75dupCACACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000470687
  ensembl transcript: ENST00000602130
  gene symbol: HNRNPUL1
  hgvsc: ENST00000602130.1:c.1266+70_1266+75dupCACACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000472315
  ensembl transcript: ENST00000595196
  gene symbol: HNRNPUL1
  hgvsc: ENST00000595196.1:c.*842+70_*842+75dupCACACA
  variant of: http://identifiers.org/hgnc/17011
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105323
  ensembl protein: ENSP00000367460
  ensembl transcript: ENST00000378215
  gene symbol: HNRNPUL1
  hgvsc: ENST00000378215.4:c.924+70_924+75dupCACACA
  variant of: http://identifiers.org/hgnc/17011
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10662
  bin: 3.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 10857
  bin: 2.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 8395
  bin: 2.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 3.75e1
  variant carriers: 25
num of homozygotes: 0
reference allele: G

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

GenotypeDepth
all individuals: 41
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1413
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8010
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43290
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2236
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 542
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2541
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.239341085271318e-4
allele num: 16512
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

FS
type: SiteQuality
SIO_000300: 2.601e0

QD
type: SiteQuality
SIO_000300: 1.178e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 1.710499e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
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num of homozygotes: 0

East Asian
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Other
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African
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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FS
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MQ
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QD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

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

European (Non-Finnish)
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Other
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South Asian
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allele frequency: 6.056935190793458e-5
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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African
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QD
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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num of homozygotes: 0

Latino
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Other
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FS
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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QD
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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African
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MQ
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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FS
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MQRankSum
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DP
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

South Asian
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allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

Latino
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allele num: 11558
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 3.000120004800192e-5
allele num: 66664
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66544
num of homozygotes: 0

South Asian
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European (Finnish)
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African
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Other
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FS
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MQRankSum
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MQ
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VQSLOD
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DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 1.162790697674419e-4
allele num: 8600
num of homozygotes: 0

Other
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Latino
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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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MQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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FS
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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African
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Latino
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ClippingRankSum
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MQ
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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FS
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 3.079860790292279e-5
allele num: 64938
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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QD
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ClippingRankSum
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DP
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InbreedingCoeff
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FS
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MQ
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 9.1e-1

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

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.541402059313151e-5
allele num: 64876
num of homozygotes: 0

Latino
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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QD
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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FS
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MQ
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16132
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9862
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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allele frequency: 6.25e-5
allele num: 16000
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European (Non-Finnish)
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allele frequency: 1.59169770477191e-5
allele num: 62826
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQRankSum
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MQ
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.629e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10686
num of homozygotes: 0

African
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allele frequency: 2.032933523073795e-4
allele num: 9838
num of homozygotes: 0

East Asian
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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ReadPosRankSum
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QD
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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ClippingRankSum
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 9564
num of homozygotes: 0

Latino
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South Asian
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allele num: 15712
num of homozygotes: 0

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

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

European (Finnish)
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Other
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African
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East Asian
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Latino
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allele frequency: 1.729206294310911e-4
allele num: 11566
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South Asian
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MQRankSum
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MQ
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FS
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.503e1

DP
type: SiteQuality
SIO_000300: 3.945351e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

GenotypeQuality
all individuals: 2869
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7978
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30817
bin: 9.75e1
variant carriers: 273

GenotypeQuality
all individuals: 954
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3424
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3152
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4084
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 255
allele frequency: 2.468538238141336e-2
allele num: 10330
num of homozygotes: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.54008898574412e-5
allele num: 66078
num of homozygotes: 0

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

Latino
type: Population
allele count: 16
allele frequency: 1.383365035448729e-3
allele num: 11566
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 3.95143e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.82e0

QD
type: SiteQuality
SIO_000300: 1.56e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

GenotypeQuality
all individuals: 62
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2872
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4112
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3430
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30631
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1975
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7927
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1577
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3163
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
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: 10330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66068
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14838
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.923e1

DP
type: SiteQuality
SIO_000300: 3.936852e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.25e0

VQSLOD
type: SiteQuality
SIO_000300: 2.69e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.57e-1

QD
type: SiteQuality
SIO_000300: 1.517e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.17e-1

GenotypeQuality
all individuals: 4133
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 91
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1976
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2874
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8361
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30632
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 3432
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 6
allele frequency: 6.942837306179125e-4
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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: 1
allele frequency: 9.678668215253581e-5
allele num: 10332
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: 14822
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 4.877e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.639e0

VQSLOD
type: SiteQuality
SIO_000300: 7.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.75e-1

QD
type: SiteQuality
SIO_000300: 1.539e1

DP
type: SiteQuality
SIO_000300: 3.939971e6

GenotypeQuality
all individuals: 1948
bin: 7.25e1
variant carriers: 24

GenotypeQuality
all individuals: 241
bin: 4.25e1
variant carriers: 12

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 15

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 32392
bin: 9.75e1
variant carriers: 19256

GenotypeQuality
all individuals: 8114
bin: 6.25e1
variant carriers: 18

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3390
bin: 7.75e1
variant carriers: 26

GenotypeQuality
all individuals: 808
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 272
bin: 4.75e1
variant carriers: 34

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 34

GenotypeQuality
all individuals: 4072
bin: 6.75e1
variant carriers: 35

GenotypeQuality
all individuals: 3139
bin: 8.25e1
variant carriers: 32

GenotypeQuality
all individuals: 388
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2843
bin: 9.25e1
variant carriers: 27

GenotypeQuality
all individuals: 648
bin: 3.25e1
variant carriers: 13

GenotypeQuality
all individuals: 1569
bin: 8.75e1
variant carriers: 18

East Asian
type: Population
allele count: 3100
allele frequency: 3.590456335418115e-1
allele num: 8634
num of homozygotes: 588

European (Non-Finnish)
type: Population
allele count: 10474
allele frequency: 1.581315296817441e-1
allele num: 66236
num of homozygotes: 833

South Asian
type: Population
allele count: 2478
allele frequency: 1.625770896207847e-1
allele num: 15242
num of homozygotes: 213

Other
type: Population
allele count: 171
allele frequency: 1.930022573363431e-1
allele num: 886
num of homozygotes: 17

Latino
type: Population
allele count: 1612
allele frequency: 1.393740273214595e-1
allele num: 11566
num of homozygotes: 125

African
type: Population
allele count: 2908
allele frequency: 2.807491793782583e-1
allele num: 10358
num of homozygotes: 407

European (Finnish)
type: Population
allele count: 1016
allele frequency: 1.536135470214696e-1
allele num: 6614
num of homozygotes: 68

DP
type: SiteQuality
SIO_000300: 4.394177e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.18e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.77e-1

FS
type: SiteQuality
SIO_000300: 2.448e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 3.4e0

QD
type: SiteQuality
SIO_000300: 1.476e1

GenotypeQuality
all individuals: 14433
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8021
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3916
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3274
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17298
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4779
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3082
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1898
bin: 8.75e1
variant carriers: 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: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15274
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509388395822013e-5
allele num: 66252
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.525e0

QD
type: SiteQuality
SIO_000300: 1.249e1

MQRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.923e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.47e-1

MQ
type: SiteQuality
SIO_000300: 5.848e1

DP
type: SiteQuality
SIO_000300: 2.775655e6

GenotypeQuality
all individuals: 205
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14430
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3278
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1899
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4804
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3926
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3097
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8088
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18586
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.646922631680494e-5
allele num: 10366
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
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: 15492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66342
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.339e0

FS
type: SiteQuality
SIO_000300: 5.321e0

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-1

QD
type: SiteQuality
SIO_000300: 1.352e1

VQSLOD
type: SiteQuality
SIO_000300: 5.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.379e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

DP
type: SiteQuality
SIO_000300: 2.787848e6

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8095
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18822
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1901
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3098
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3923
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 162
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14429
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4801
bin: 7.75e1
variant carriers: 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: 10366
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.52106817770812e-5
allele num: 66356
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.32e-1

QD
type: SiteQuality
SIO_000300: 1.261e1

FS
type: SiteQuality
SIO_000300: 6.91e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: 6.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-2

DP
type: SiteQuality
SIO_000300: 2.79058e6

GenotypeQuality
all individuals: 14428
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 121
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4806
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 254
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19161
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8106
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1901
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3277
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.506205566935775e-5
allele num: 66392
num of homozygotes: 0

East Asian
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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MQ
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FS
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VQSLOD
type: SiteQuality
SIO_000300: 5.25e-1

QD
type: SiteQuality
SIO_000300: 1.168e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.94e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

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

African
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South Asian
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European (Non-Finnish)
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allele frequency: 1.505117399157134e-5
allele num: 66440
num of homozygotes: 0

Latino
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East Asian
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allele frequency: 0.0e0
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Other
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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ReadPosRankSum
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FS
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: -1.355e0

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

European (Non-Finnish)
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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African
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Other
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South Asian
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allele num: 16512
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Latino
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num of homozygotes: 0

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

DP
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SIO_000300: 2.81798e6

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

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

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

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

Other
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num of homozygotes: 0

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

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

South Asian
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allele num: 16512
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MQRankSum
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SIO_000300: 2.2e-1

BaseQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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MQ
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FS
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SIO_000300: 5.966e0

ReadPosRankSum
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QD
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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Other
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Latino
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num of homozygotes: 0

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

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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South Asian
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Latino
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European (Finnish)
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East Asian
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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InbreedingCoeff
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DP
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MQ
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Latino
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African
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East Asian
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European (Non-Finnish)
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South Asian
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MQ
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DP
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.75e1
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South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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European (Finnish)
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Other
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African
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.495055439017081e-5
allele num: 66740
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.124e0

MQRankSum
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SIO_000300: -2.08e-1

ClippingRankSum
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SIO_000300: -1.72e-1

ReadPosRankSum
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SIO_000300: 4.43e-1

BaseQRankSum
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DP
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SIO_000300: 2.818169e6

QD
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SIO_000300: 1.321e1

InbreedingCoeff
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SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 2.16e0

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -2.09e-1

ReadPosRankSum
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QD
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BaseQRankSum
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FS
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MQ
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InbreedingCoeff
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VQSLOD
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SIO_000300: 3.74e0

MQRankSum
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SIO_000300: 3.5e-1

DP
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SIO_000300: 2.817909e6

GenotypeDepth
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variant carriers: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

Latino
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MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

MQ
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SIO_000300: 5.959e1

BaseQRankSum
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ReadPosRankSum
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FS
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SIO_000300: 0.0e0

InbreedingCoeff
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VQSLOD
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QD
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SIO_000300: 1.181e1

DP
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SIO_000300: 2.81788e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

Other
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num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.177e-1

FS
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SIO_000300: 1.714e0

MQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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QD
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BaseQRankSum
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SIO_000300: 4.75e0

ReadPosRankSum
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SIO_000300: 1.76e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 8.990380293086398e-5
allele num: 66738
num of homozygotes: 0

East Asian
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South Asian
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African
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allele num: 10404
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European (Finnish)
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allele count: 0
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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QD
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ReadPosRankSum
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InbreedingCoeff
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MQ
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GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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African
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Other
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQ
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QD
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VQSLOD
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele num: 8654
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South Asian
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Latino
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European (Non-Finnish)
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FS
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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VQSLOD
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QD
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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East Asian
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European (Finnish)
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Latino
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VQSLOD
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

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

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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African
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Other
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South Asian
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allele frequency: 1.029928510844541e-3
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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FS
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QD
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BaseQRankSum
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MQ
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DP
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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ClippingRankSum
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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FS
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

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

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

Latino
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European (Non-Finnish)
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East Asian
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African
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Other
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South Asian
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VQSLOD
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QD
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MQ
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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South Asian
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African
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Latino
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European (Non-Finnish)
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European (Finnish)
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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FS
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DP
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QD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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South Asian
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East Asian
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FS
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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MQ
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ReadPosRankSum
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DP
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66374
num of homozygotes: 0

South Asian
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allele frequency: 5.467800729040097e-4
allele num: 16460
num of homozygotes: 0

MQRankSum
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SIO_000300: -9.360000000000001e-1

ReadPosRankSum
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FS
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SIO_000300: 2.595e0

InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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MQ
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SIO_000300: 5.967e1

BaseQRankSum
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SIO_000300: 4.64e0

ClippingRankSum
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SIO_000300: 2.34e-1

DP
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QD
type: SiteQuality
SIO_000300: 1.517e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
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num of homozygotes: 0

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

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

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

African
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allele count: 2
allele frequency: 1.955034213098729e-4
allele num: 10230
num of homozygotes: 0

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

East Asian
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.93e-1

MQRankSum
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BaseQRankSum
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MQ
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QD
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ClippingRankSum
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InbreedingCoeff
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DP
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FS
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SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 1.74e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

East Asian
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allele num: 8628
num of homozygotes: 0

Other
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num of homozygotes: 0

Latino
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num of homozygotes: 0

MQRankSum
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SIO_000300: -3.2e-2

FS
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SIO_000300: 4.193e0

InbreedingCoeff
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SIO_000300: 9.0e-4

ReadPosRankSum
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BaseQRankSum
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DP
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VQSLOD
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MQ
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SIO_000300: 5.963e1

QD
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ClippingRankSum
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SIO_000300: -4.67e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.016500256402522e-5
allele num: 66302
num of homozygotes: 0

South Asian
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num of homozygotes: 0

African
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VQSLOD
type: SiteQuality
SIO_000300: -2.187e0

DP
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SIO_000300: 2.803983e6

ReadPosRankSum
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SIO_000300: 1.25e0

InbreedingCoeff
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MQ
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SIO_000300: 5.981e1

MQRankSum
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SIO_000300: 2.06e-1

FS
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SIO_000300: 1.5704e1

ClippingRankSum
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SIO_000300: -1.571e0

QD
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BaseQRankSum
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SIO_000300: 1.51e-1

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 31
allele frequency: 2.690972222222222e-3
allele num: 11520
num of homozygotes: 0

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

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

Other
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South Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.57e-1

ReadPosRankSum
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MQ
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BaseQRankSum
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FS
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SIO_000300: 5.31e-1

InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
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MQRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.514050387596899e-5
allele num: 66048
num of homozygotes: 0

East Asian
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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South Asian
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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MQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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DP
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QD
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

African
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allele frequency: 9.891196834817012e-5
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num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65972
num of homozygotes: 0

European (Finnish)
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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: 16356
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.741250217656277e-4
allele num: 11486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10100
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.025e0

DP
type: SiteQuality
SIO_000300: 2.788942e6

QD
type: SiteQuality
SIO_000300: 1.406e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.98e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.053e0

FS
type: SiteQuality
SIO_000300: 1.459e0

VQSLOD
type: SiteQuality
SIO_000300: 2.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.05e-1

GenotypeQuality
all individuals: 1897
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515840533575868e-5
allele num: 65970
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: 16356
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

QD
type: SiteQuality
SIO_000300: 1.186e1

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

DP
type: SiteQuality
SIO_000300: 2.787976e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

FS
type: SiteQuality
SIO_000300: 7.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.814e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 18831
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65932
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

DP
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SIO_000300: 2.781658e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.428e0

MQRankSum
type: SiteQuality
SIO_000300: -6.8e-1

QD
type: SiteQuality
SIO_000300: 1.424e1

FS
type: SiteQuality
SIO_000300: 1.584e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.316e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 5.913e1

VQSLOD
type: SiteQuality
SIO_000300: 3.22e0

GenotypeQuality
all individuals: 14316
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1887
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variant carriers: 0

GenotypeQuality
all individuals: 4754
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10092
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 1.517220452131695e-5
allele num: 65910
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.896e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.55e-1

FS
type: SiteQuality
SIO_000300: 1.482e0

DP
type: SiteQuality
SIO_000300: 2.777711e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-2

QD
type: SiteQuality
SIO_000300: 1.203e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

GenotypeQuality
all individuals: 104
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4392
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 12521
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.164958061509786e-4
allele num: 8584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
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: 9996
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65524
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

MQ
type: SiteQuality
SIO_000300: 5.745e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.624e0

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

MQRankSum
type: SiteQuality
SIO_000300: -1.08e-1

DP
type: SiteQuality
SIO_000300: 2.719062e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3185
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GenotypeQuality
all individuals: 14170
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 8.821453775582216e-5
allele num: 11336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15046
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.408e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.43e-1

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.841e1

DP
type: SiteQuality
SIO_000300: 2.699029e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.21e-1

FS
type: SiteQuality
SIO_000300: 5.822e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.186e0

GenotypeQuality
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variant carriers: 18

GenotypeQuality
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GenotypeQuality
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variant carriers: 19

GenotypeQuality
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GenotypeQuality
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variant carriers: 15

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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bin: 9.75e1
variant carriers: 1320

South Asian
type: Population
allele count: 105
allele frequency: 9.083044982698962e-3
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 345
allele frequency: 3.73538328280641e-2
allele num: 9236
num of homozygotes: 0

Other
type: Population
allele count: 12
allele frequency: 1.570680628272251e-2
allele num: 764
num of homozygotes: 0

Latino
type: Population
allele count: 52
allele frequency: 5.138339920948616e-3
allele num: 10120
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 198
allele frequency: 3.468815697266994e-2
allele num: 5708
num of homozygotes: 0

East Asian
type: Population
allele count: 34
allele frequency: 4.221504842314378e-3
allele num: 8054
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 806
allele frequency: 1.391766818621356e-2
allele num: 57912
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

MQRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.92e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.44e0

QD
type: SiteQuality
SIO_000300: 8.800000000000001e0

DP
type: SiteQuality
SIO_000300: 1.939927e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 26

GenotypeQuality
all individuals: 1022
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 973
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.590136759220887e-4
allele num: 57912
num of homozygotes: 0

African
type: Population
allele count: 17
allele frequency: 1.84062364660026e-3
allele num: 9236
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.730103806228374e-4
allele num: 11560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.976284584980237e-4
allele num: 10120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8054
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5708
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

DP
type: SiteQuality
SIO_000300: 1.939927e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -7.7e-2

MQ
type: SiteQuality
SIO_000300: 5.92e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1