1-24973205-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24973205
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24973205
    reference: chr 1
allele count: 2
allele frequency: 1.64923970049807e-5
allele num: 121268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.181A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.159A>G
  hgvsp: ENST00000600523.1:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.178A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.159A>G
  hgvsp: ENST00000374389.4:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000466910
  gene symbol: SRRM1
  hgvsc: ENST00000466910.1:n.214A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.159A>G
  hgvsp: ENST00000323848.9:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.42A>G
  hgvsp: ENST00000593639.1:c.42A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.159A>G
  hgvsp: ENST00000447431.2:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.42A>G
  hgvsp: ENST00000596378.1:c.42A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.211A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.172A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.193A>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Thr53Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

1-24973217-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24973217
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24973217
    reference: chr 1
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.184G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.171G>A
  hgvsp: ENST00000447431.2:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.171G>A
  hgvsp: ENST00000600523.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.171G>A
  hgvsp: ENST00000374389.4:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.205G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.223G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.54G>A
  hgvsp: ENST00000596378.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.171G>A
  hgvsp: ENST00000323848.9:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.54G>A
  hgvsp: ENST00000593639.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.190G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.193G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000466910
  gene symbol: SRRM1
  hgvsc: ENST00000466910.1:n.226G>A
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7727
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr57Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

1-24973257-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24973257
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24973257
    reference: chr 1
allele count: 1
allele frequency: 8.262414277451872e-6
allele num: 121030
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000466910
  gene symbol: SRRM1
  hgvsc: ENST00000466910.1:n.266A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.94A>G
  hgvsp: ENSP00000469151.1:p.Ile32Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.263A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.211A>G
  hgvsp: ENSP00000326261.8:p.Ile71Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.230A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.224A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.245A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.94A>G
  hgvsp: ENSP00000471084.1:p.Ile32Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.211A>G
  hgvsp: ENSP00000471819.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.211A>G
  hgvsp: ENSP00000363510.3:p.Ile71Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.211A>G
  hgvsp: ENSP00000391430.2:p.Ile71Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.233A>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile71Val
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

1-24973269-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24973269
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24973269
    reference: chr 1
allele count: 1
allele frequency: 8.295175525914129e-6
allele num: 120552
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.275C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000466910
  gene symbol: SRRM1
  hgvsc: ENST00000466910.1:n.278C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.223C>T
  hgvsp: ENST00000600523.1:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.223C>T
  hgvsp: ENST00000447431.2:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.106C>T
  hgvsp: ENST00000596378.1:c.106C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.236C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.106C>T
  hgvsp: ENST00000593639.1:c.106C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.257C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.223C>T
  hgvsp: ENST00000323848.9:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.245C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.223C>T
  hgvsp: ENST00000374389.4:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.242C>T
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu75Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-24973284-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24973284
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24973284
    reference: chr 1
allele count: 4
allele frequency: 3.338006542492823e-5
allele num: 119832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.234+4C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.117+4C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.272C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.117+4C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.247+4C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.253+4C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.234+4C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.256+4C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000466910
  gene symbol: SRRM1
  hgvsc: ENST00000466910.1:n.289+4C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.286+4C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.234+4C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.234+4C>A
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.234+4C>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

1-24973290-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24973290
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24973290
    reference: chr 1
allele count: 4
allele frequency: 3.344481605351171e-5
allele num: 119600
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.286+10T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.256+10T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.234+10T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.278T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.234+10T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.247+10T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000466910
  gene symbol: SRRM1
  hgvsc: ENST00000466910.1:n.289+10T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.253+10T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.234+10T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.234+10T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.117+10T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.117+10T>C
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7726
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

1-24973294-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24973294
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24973294
    reference: chr 1
allele count: 5
allele frequency: 4.186903366270307e-5
allele num: 119420
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.282A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.234+14A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.234+14A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.117+14A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.256+14A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.247+14A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.286+14A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.234+14A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.117+14A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.234+14A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000466910
  gene symbol: SRRM1
  hgvsc: ENST00000466910.1:n.289+14A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.253+14A>G
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4881
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-24973298-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24973298
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24973298
    reference: chr 1
allele count: 2
allele frequency: 1.677711601375723e-5
allele num: 119210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000466910
  gene symbol: SRRM1
  hgvsc: ENST00000466910.1:n.289+18G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.286G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.117+18G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.117+18G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.256+18G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.234+18G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.253+18G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.247+18G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.234+18G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.286+18G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.234+18G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.234+18G>T
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

1-24973300-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24973300
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24973300
    reference: chr 1
allele count: 1
allele frequency: 8.392077878482712e-6
allele num: 119160
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.117+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.288T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.117+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.234+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.256+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000466910
  gene symbol: SRRM1
  hgvsc: ENST00000466910.1:n.289+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.253+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.234+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.286+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.234+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.247+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.234+20T>C
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7725
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

1-24973301-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24973301
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24973301
    reference: chr 1
allele count: 1
allele frequency: 8.402937667008386e-6
allele num: 119006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.234+21C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.286+21C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.117+21C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.234+21C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.117+21C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.247+21C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000466910
  gene symbol: SRRM1
  hgvsc: ENST00000466910.1:n.289+21C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.256+21C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.234+21C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.253+21C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.234+21C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.289C>T
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

1-24973319-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24973319
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24973319
    reference: chr 1
allele count: 2
allele frequency: 1.695835029168363e-5
allele num: 117936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.253+39A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.234+39A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.234+39A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.234+39A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000466910
  gene symbol: SRRM1
  hgvsc: ENST00000466910.1:n.289+39A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.286+39A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.117+39A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.307A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.117+39A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.247+39A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.234+39A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.256+39A>T
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6624
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-24973322-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24973322
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24973322
    reference: chr 1
allele count: 1
allele frequency: 8.490838385382172e-6
allele num: 117774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.234+42T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.117+42T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.234+42T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.234+42T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.234+42T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.256+42T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.310T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.253+42T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000466910
  gene symbol: SRRM1
  hgvsc: ENST00000466910.1:n.289+42T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.117+42T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.247+42T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.286+42T>C
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4881
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7723
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

1-24973520-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24973520
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24973520
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 2720
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.286+240G>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.508G>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.117+240G>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.257-50G>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.253+240G>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.235-50G>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.234+240G>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000466910
  gene symbol: SRRM1
  hgvsc: ENST00000466910.1:n.290-50G>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.234+240G>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.117+240G>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.234+240G>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.247+240G>C
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19170
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS

1-24975305-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975305
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975305
    reference: chr 1
allele count: 2
allele frequency: 1.668641225450116e-5
allele num: 119858
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.197G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2293G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.248-45G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.235-45G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.254-45G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.235-45G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.118-45G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.*268-45G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.387-45G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.118-45G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.287-45G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.281G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.235-45G>A
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10450
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10070
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

1-24975305-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975305
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975305
    reference: chr 1
allele count: 22
allele frequency: 1.835505347995128e-4
allele num: 119858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.197G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.248-45G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.235-45G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.118-45G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.287-45G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2293G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.235-45G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.235-45G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.281G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.118-45G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.254-45G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.387-45G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.*268-45G>T
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10070
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7192
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8656
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10450
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6601
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

1-24975319-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975319
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975319
    reference: chr 1
allele count: 1
allele frequency: 8.322652595835345e-6
allele num: 120154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.*268-31C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.118-31C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.248-31C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.295C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.235-31C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.118-31C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.387-31C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2307C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.254-31C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.287-31C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.211C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.235-31C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.235-31C>T
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9256
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

1-24975330-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975330
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975330
    reference: chr 1
allele count: 1
allele frequency: 8.296827293243064e-6
allele num: 120528
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.235-20C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.248-20C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2318C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.222C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.118-20C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.235-20C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.*268-20C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.387-20C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.254-20C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.306C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.287-20C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.118-20C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.235-20C>T
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

1-24975335-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975335
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975335
    reference: chr 1
allele count: 15
allele frequency: 1.242174301898042e-4
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.118-15C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.235-15C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.235-15C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.227C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2323C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.248-15C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.311C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.235-15C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.287-15C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.254-15C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.387-15C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.*268-15C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.118-15C>T
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8737
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-24975336-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975336
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975336
    reference: chr 1
allele count: 1
allele frequency: 8.276912380605539e-6
allele num: 120818
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2324G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.118-14G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.235-14G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.387-14G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.235-14G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.235-14G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.312G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.248-14G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.254-14G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.228G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.*268-14G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.287-14G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.118-14G>A
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9920
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-24975337-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975337
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975337
    reference: chr 1
allele count: 1
allele frequency: 8.273762245168123e-6
allele num: 120864
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.235-13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471819
  ensembl transcript: ENST00000600523
  gene symbol: SRRM1
  hgvsc: ENST00000600523.1:c.*268-13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2325T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.313T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.235-13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.229T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.287-13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.118-13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.387-13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.248-13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.235-13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.254-13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.118-13T>C
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

1-24975382-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975382
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975382
    reference: chr 1
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.358G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.267G>A
  hgvsp: ENST00000374389.4:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.150G>A
  hgvsp: ENST00000596378.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.274G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.267G>A
  hgvsp: ENST00000323848.9:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.150G>A
  hgvsp: ENST00000593639.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.267G>A
  hgvsp: ENST00000447431.2:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.319G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2370G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.280G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.419G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.286G>A
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu89Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum

1-24975409-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975409
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975409
    reference: chr 1
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.294T>C
  hgvsp: ENST00000374389.4:c.294T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.177T>C
  hgvsp: ENST00000596378.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.294T>C
  hgvsp: ENST00000447431.2:c.294T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.294T>C
  hgvsp: ENST00000323848.9:c.294T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.177T>C
  hgvsp: ENST00000593639.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.307T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.346T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.385T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.446T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.301T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.313T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2397T>C
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala98Ala
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

1-24975430-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975430
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975430
    reference: chr 1
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.467G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.198G>A
  hgvsp: ENST00000593639.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2418G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.198G>A
  hgvsp: ENST00000596378.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.334G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.328G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.315G>A
  hgvsp: ENST00000447431.2:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.315G>A
  hgvsp: ENST00000374389.4:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.406G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.367G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.315G>A
  hgvsp: ENST00000323848.9:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.12G>A
  hgvsp: ENST00000537199.1:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.322G>A
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11273
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu105Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-24975442-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975442
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975442
    reference: chr 1
allele count: 3
allele frequency: 2.472187886279357e-5
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.327G>T
  hgvsp: ENST00000374389.4:c.327G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.210G>T
  hgvsp: ENST00000596378.1:c.210G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.327G>T
  hgvsp: ENST00000447431.2:c.327G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.210G>T
  hgvsp: ENST00000593639.1:c.210G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.418G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.346G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2430G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.379G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.340G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.479G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.327G>T
  hgvsp: ENST00000323848.9:c.327G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.24G>T
  hgvsp: ENST00000537199.1:c.24G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.334G>T
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu109Leu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

1-24975445-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975445
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975445
    reference: chr 1
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.482A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.213A>G
  hgvsp: ENST00000596378.1:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.27A>G
  hgvsp: ENST00000537199.1:c.27A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.349A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.337A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.330A>G
  hgvsp: ENST00000323848.9:c.330A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.421A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.330A>G
  hgvsp: ENST00000447431.2:c.330A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.382A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.213A>G
  hgvsp: ENST00000593639.1:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.343A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2433A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.330A>G
  hgvsp: ENST00000374389.4:c.330A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11165
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu110Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

1-24975451-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975451
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975451
    reference: chr 1
allele count: 2
allele frequency: 1.648424106554134e-5
allele num: 121328
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.336A>G
  hgvsp: ENST00000447431.2:c.336A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.336A>G
  hgvsp: ENST00000323848.9:c.336A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.33A>G
  hgvsp: ENST00000537199.1:c.33A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.427A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.219A>G
  hgvsp: ENST00000593639.1:c.219A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2439A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.488A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.343A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.336A>G
  hgvsp: ENST00000374389.4:c.336A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.349A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.219A>G
  hgvsp: ENST00000596378.1:c.219A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.388A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.355A>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala112Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

1-24975460-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975460
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975460
    reference: chr 1
allele count: 2
allele frequency: 1.648967746190884e-5
allele num: 121288
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.228C>T
  hgvsp: ENST00000596378.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.358C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.228C>T
  hgvsp: ENST00000593639.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.345C>T
  hgvsp: ENST00000374389.4:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.436C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.345C>T
  hgvsp: ENST00000447431.2:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2448C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.345C>T
  hgvsp: ENST00000323848.9:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.497C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.364C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.42C>T
  hgvsp: ENST00000537199.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.352C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.397C>T
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn115Asn
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

1-24975461-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975461
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975461
    reference: chr 1
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.229A>G
  hgvsp: ENSP00000471084.1:p.Ile77Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2449A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.346A>G
  hgvsp: ENSP00000363510.3:p.Ile116Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.398A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.43A>G
  hgvsp: ENSP00000441776.1:p.Ile15Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.229A>G
  hgvsp: ENSP00000469151.1:p.Ile77Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.498A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.353A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.365A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.346A>G
  hgvsp: ENSP00000326261.8:p.Ile116Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.346A>G
  hgvsp: ENSP00000391430.2:p.Ile116Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.437A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.359A>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile116Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

1-24975463-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975463
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975463
    reference: chr 1
allele count: 3
allele frequency: 2.473981956424931e-5
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.348C>T
  hgvsp: ENST00000323848.9:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.231C>T
  hgvsp: ENST00000593639.1:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.500C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.355C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.231C>T
  hgvsp: ENST00000596378.1:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.439C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.45C>T
  hgvsp: ENST00000537199.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.348C>T
  hgvsp: ENST00000447431.2:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2451C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.348C>T
  hgvsp: ENST00000374389.4:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.361C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.367C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.400C>T
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile116Ile
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

1-24975465-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975465
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975465
    reference: chr 1
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.233C>T
  hgvsp: ENSP00000469151.1:p.Ala78Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.233C>T
  hgvsp: ENSP00000471084.1:p.Ala78Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2453C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.502C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.47C>T
  hgvsp: ENSP00000441776.1:p.Ala16Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.369C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.350C>T
  hgvsp: ENSP00000363510.3:p.Ala117Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.402C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.363C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.350C>T
  hgvsp: ENSP00000391430.2:p.Ala117Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.350C>T
  hgvsp: ENSP00000326261.8:p.Ala117Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.357C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.441C>T
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala117Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

1-24975466-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975466
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975466
    reference: chr 1
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.370G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.48G>T
  hgvsp: ENST00000537199.1:c.48G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.403G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.503G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.442G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.351G>T
  hgvsp: ENST00000447431.2:c.351G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2454G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.351G>T
  hgvsp: ENST00000374389.4:c.351G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.234G>T
  hgvsp: ENST00000596378.1:c.234G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.234G>T
  hgvsp: ENST00000593639.1:c.234G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.351G>T
  hgvsp: ENST00000323848.9:c.351G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.358G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.364G>T
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala117Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

1-24975481-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975481
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975481
    reference: chr 1
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.249T>C
  hgvsp: ENST00000596378.1:c.249T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.366T>C
  hgvsp: ENST00000323848.9:c.366T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2469T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.518T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.366T>C
  hgvsp: ENST00000374389.4:c.366T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.418T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.366T>C
  hgvsp: ENST00000447431.2:c.366T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.373T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.379T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.249T>C
  hgvsp: ENST00000593639.1:c.249T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.457T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.385T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.63T>C
  hgvsp: ENST00000537199.1:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8744
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala122Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-24975484-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975484
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975484
    reference: chr 1
allele count: 1
allele frequency: 8.266102367411717e-6
allele num: 120976
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2472C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.388C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.66C>T
  hgvsp: ENST00000537199.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.369C>T
  hgvsp: ENST00000374389.4:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.460C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.369C>T
  hgvsp: ENST00000447431.2:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.369C>T
  hgvsp: ENST00000323848.9:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.382C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.252C>T
  hgvsp: ENST00000596378.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.252C>T
  hgvsp: ENST00000593639.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.376C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.421C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.521C>T
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8742
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe123Phe
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

1-24975488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975488
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975488
    reference: chr 1
allele count: 2
allele frequency: 1.654971534489607e-5
allele num: 120848
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.256G>A
  hgvsp: ENSP00000471084.1:p.Glu86Lys
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.392G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.70G>A
  hgvsp: ENSP00000441776.1:p.Glu24Lys
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.373G>A
  hgvsp: ENSP00000391430.2:p.Glu125Lys
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.386G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.525G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.425G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2476G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.464G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.256G>A
  hgvsp: ENSP00000469151.1:p.Glu86Lys
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.373G>A
  hgvsp: ENSP00000326261.8:p.Glu125Lys
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.373G>A
  hgvsp: ENSP00000363510.3:p.Glu125Lys
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.380G>A
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu125Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

1-24975510-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975510
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975510
    reference: chr 1
allele count: 1
allele frequency: 8.313242996092776e-6
allele num: 120290
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.278A>G
  hgvsp: ENSP00000471084.1:p.Lys93Arg
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.395A>G
  hgvsp: ENSP00000326261.8:p.Lys132Arg
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.402A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.408A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.486A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.547A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.395A>G
  hgvsp: ENSP00000391430.2:p.Lys132Arg
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.395A>G
  hgvsp: ENSP00000363510.3:p.Lys132Arg
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.278A>G
  hgvsp: ENSP00000469151.1:p.Lys93Arg
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2498A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.414A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.92A>G
  hgvsp: ENSP00000441776.1:p.Lys31Arg
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.447A>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys132Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

1-24975522-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975522
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975522
    reference: chr 1
allele count: 6
allele frequency: 5.009434434852305e-5
allele num: 119774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+2T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+2T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+2T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+2T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+2T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+2T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+2T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+2T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+2T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+2T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+2T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+2T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+2T>C
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.405+2T>C
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-24975524-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975524
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975524
    reference: chr 1
allele count: 1
allele frequency: 8.351009637065121e-6
allele num: 119746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+4A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+4A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+4A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+4A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+4A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+4A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+4A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+4A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+4A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+4A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+4A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+4A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+4A>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.405+4A>G
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

1-24975528-CCTTTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975528
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975523
    reference: chr 1
allele count: 1
allele frequency: 8.360924383799873e-6
allele num: 119604
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+16_424+20delTTTCT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+16_557+20delTTTCT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+16_418+20delTTTCT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+16_405+20delTTTCT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+16_2508+20delTTTCT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+16_496+20delTTTCT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+16_405+20delTTTCT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+16_412+20delTTTCT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+16_457+20delTTTCT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+16_405+20delTTTCT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+16_288+20delTTTCT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+16_102+20delTTTCT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+16_288+20delTTTCT
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: CCTTTT
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

1-24975529-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975529
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975529
    reference: chr 1
allele count: 1
allele frequency: 8.369741709770836e-6
allele num: 119478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+9C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+9C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+9C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+9C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+9C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+9C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+9C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+9C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+9C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+9C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+9C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+9C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+9C>T
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10835
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

1-24975531-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975531
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975531
    reference: chr 1
allele count: 1
allele frequency: 8.37058242512514e-6
allele num: 119466
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+11T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+11T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+11T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+11T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+11T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+11T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+11T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+11T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+11T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+11T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+11T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+11T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+11T>C
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

1-24975533-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975533
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975533
    reference: chr 1
allele count: 1
allele frequency: 8.376331836762046e-6
allele num: 119384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+13T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+13T>C
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

1-24975534-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975534
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975534
    reference: chr 1
allele count: 1
allele frequency: 8.378296859814337e-6
allele num: 119356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+14C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+14C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+14C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+14C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+14C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+14C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+14C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+14C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+14C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+14C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+14C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+14C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+14C>T
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD

1-24975540-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975540
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975540
    reference: chr 1
allele count: 1
allele frequency: 8.403220113947665e-6
allele num: 119002
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+20T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+20T>C
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10649
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: DP

1-24975545-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975545
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975545
    reference: chr 1
allele count: 1
allele frequency: 8.419634587858886e-6
allele num: 118770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+25T>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+25T>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+25T>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+25T>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+25T>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+25T>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+25T>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+25T>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+25T>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+25T>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+25T>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+25T>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+25T>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8611
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

1-24975548-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975548
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975548
    reference: chr 1
allele count: 15
allele frequency: 1.26437169156074e-4
allele num: 118636
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+28C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+28C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+28C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+28C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+28C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+28C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+28C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+28C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+28C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+28C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+28C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+28C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+28C>T
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8599
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

1-24975549-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975549
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975549
    reference: chr 1
allele count: 4
allele frequency: 3.373762250974174e-5
allele num: 118562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+29G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+29G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+29G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+29G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+29G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+29G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+29G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+29G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+29G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+29G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+29G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+29G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+29G>A
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8661
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

1-24975549-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975549
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975549
    reference: chr 1
allele count: 1
allele frequency: 8.434405627435435e-6
allele num: 118562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+29G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+29G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+29G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+29G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+29G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+29G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+29G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+29G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+29G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+29G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+29G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+29G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+29G>T
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10490
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

1-24975569-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975569
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975569
    reference: chr 1
allele count: 1
allele frequency: 8.51469636592759e-6
allele num: 117444
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+49G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+49G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+49G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+49G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+49G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+49G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+49G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+49G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+49G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+49G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+49G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+49G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+49G>A
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/1-24975570-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24975570
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24975570
    reference: chr 1
allele count: 1
allele frequency: 8.518758305789349e-6
allele num: 117388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.457+50C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.557+50C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.405+50C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.412+50C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2508+50C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.405+50C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.288+50C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.496+50C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.418+50C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.405+50C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.424+50C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.288+50C>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.102+50C>A
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8213
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS

1-24976420-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976420
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976420
    reference: chr 1
allele count: 2
allele frequency: 7.256367462448299e-5
allele num: 27562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.425-42A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.103-42A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.406-42A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.289-42A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.406-42A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.458-42A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2509-42A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.558-42A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.413-42A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.419-42A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.406-42A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.497-42A>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.289-42A>T
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20638
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6060
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24970
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD

1-24976427-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976427
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976427
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 28084
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.289-35C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.558-35C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.413-35C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.419-35C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.289-35C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.406-35C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.406-35C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.458-35C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.497-35C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2509-35C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.406-35C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.425-35C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.103-35C>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18820
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26502
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

1-24976429-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976429
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976429
    reference: chr 1
allele count: 1
allele frequency: 3.482379161443098e-5
allele num: 28716
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.419-33A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.103-33A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.406-33A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.406-33A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.289-33A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.497-33A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.458-33A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.425-33A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.558-33A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.413-33A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2509-33A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.289-33A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.406-33A>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18023
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

1-24976430-CTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976430
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976428
    reference: chr 1
allele count: 11
allele frequency: 3.816793893129771e-4
allele num: 28820
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.458-30_458-29delAT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.558-30_558-29delAT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.413-30_413-29delAT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.425-30_425-29delAT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.497-30_497-29delAT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.406-30_406-29delAT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.406-30_406-29delAT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.103-30_103-29delAT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.419-30_419-29delAT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.289-30_289-29delAT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.406-30_406-29delAT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2509-30_2509-29delAT
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.289-30_289-29delAT
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17631
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6036
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27551
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: CTA
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

1-24976432-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976432
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976432
    reference: chr 1
allele count: 1
allele frequency: 3.410641200545703e-5
allele num: 29320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.289-30A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2509-30A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.425-30A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.103-30A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.406-30A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.458-30A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.558-30A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.419-30A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.289-30A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.406-30A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.406-30A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.497-30A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.413-30A>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16798
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5969
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

1-24976433-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976433
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976433
    reference: chr 1
allele count: 1
allele frequency: 3.385011170536862e-5
allele num: 29542
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.425-29T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.406-29T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.413-29T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.406-29T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.497-29T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.458-29T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.419-29T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.406-29T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2509-29T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.289-29T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.558-29T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.103-29T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.289-29T>C
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5894
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

1-24976434-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976434
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976434
    reference: chr 1
allele count: 1
allele frequency: 3.372908796546141e-5
allele num: 29648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.458-28G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.419-28G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.558-28G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.425-28G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.103-28G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.406-28G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2509-28G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.289-28G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.406-28G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.497-28G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.406-28G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.289-28G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.413-28G>A
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16020
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

1-24976452-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976452
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976452
    reference: chr 1
allele count: 4
allele frequency: 1.064679265371307e-4
allele num: 37570
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.458-10G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.406-10G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2509-10G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.413-10G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.289-10G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.497-10G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.406-10G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.289-10G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.103-10G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.558-10G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.406-10G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.419-10G>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.425-10G>T
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7776
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-24976464-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976464
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976464
    reference: chr 1
allele count: 1
allele frequency: 2.232940335834226e-5
allele num: 44784
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.560T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.291T>C
  hgvsp: ENST00000596378.1:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.408T>C
  hgvsp: ENST00000323848.9:c.408T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2511T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.291T>C
  hgvsp: ENST00000593639.1:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.499T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.408T>C
  hgvsp: ENST00000374389.4:c.408T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.408T>C
  hgvsp: ENST00000447431.2:c.408T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.421T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.427T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.460T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.415T>C
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.105T>C
  hgvsp: ENST00000537199.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.408T>C
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

1-24976465-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976465
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976465
    reference: chr 1
allele count: 1
allele frequency: 2.209749414416405e-5
allele num: 45254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.409G>A
  hgvsp: ENSP00000363510.3:p.Glu137Lys
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.461G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.409G>A
  hgvsp: ENSP00000391430.2:p.Glu137Lys
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.106G>A
  hgvsp: ENSP00000441776.1:p.Glu36Lys
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.409G>A
  hgvsp: ENSP00000326261.8:p.Glu137Lys
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.561G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.292G>A
  hgvsp: ENSP00000471084.1:p.Glu98Lys
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.292G>A
  hgvsp: ENSP00000469151.1:p.Glu98Lys
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.422G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2512G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.428G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.416G>A
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.500G>A
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11286
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu137Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

1-24976466-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976466
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976466
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 45862
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.501A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.293A>G
  hgvsp: ENSP00000471084.1:p.Glu98Gly
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.410A>G
  hgvsp: ENSP00000326261.8:p.Glu137Gly
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.423A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.107A>G
  hgvsp: ENSP00000441776.1:p.Glu36Gly
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.410A>G
  hgvsp: ENSP00000391430.2:p.Glu137Gly
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2513A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.293A>G
  hgvsp: ENSP00000469151.1:p.Glu98Gly
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.562A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.410A>G
  hgvsp: ENSP00000363510.3:p.Glu137Gly
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.462A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.417A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.429A>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32462
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu137Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

1-24976470-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976470
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976470
    reference: chr 1
allele count: 1
allele frequency: 2.090388394163635e-5
allele num: 47838
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2517A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.466A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.414A>G
  hgvsp: ENST00000323848.9:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.297A>G
  hgvsp: ENST00000593639.1:c.297A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.414A>G
  hgvsp: ENST00000447431.2:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.297A>G
  hgvsp: ENST00000596378.1:c.297A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.421A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.566A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.505A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.111A>G
  hgvsp: ENST00000537199.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.414A>G
  hgvsp: ENST00000374389.4:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.433A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.427A>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32025
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12480
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln138Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

1-24976473-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976473
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976473
    reference: chr 1
allele count: 1
allele frequency: 2.037821975872188e-5
allele num: 49072
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.300A>G
  hgvsp: ENST00000593639.1:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.417A>G
  hgvsp: ENST00000374389.4:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.508A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.469A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.569A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2520A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.436A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.417A>G
  hgvsp: ENST00000447431.2:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.300A>G
  hgvsp: ENST00000596378.1:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.430A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.417A>G
  hgvsp: ENST00000323848.9:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.424A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.114A>G
  hgvsp: ENST00000537199.1:c.114A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu139Glu
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

1-24976477-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976477
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976477
    reference: chr 1
allele count: 1
allele frequency: 1.991952511852117e-5
allele num: 50202
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.421C>T
  hgvsp: ENST00000323848.9:c.421C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.428C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.421C>T
  hgvsp: ENST00000447431.2:c.421C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.304C>T
  hgvsp: ENST00000596378.1:c.304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2524C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.473C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.421C>T
  hgvsp: ENST00000374389.4:c.421C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.434C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000469151
  ensembl transcript: ENST00000593639
  gene symbol: SRRM1
  hgvsc: ENST00000593639.1:c.304C>T
  hgvsp: ENST00000593639.1:c.304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.512C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.118C>T
  hgvsp: ENST00000537199.1:c.118C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.440C>T
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.573C>T
  variant of: http://identifiers.org/hgnc/16638
canonical: false
consequence: incomplete terminal codon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter102Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

1-24976486-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976486
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976486
    reference: chr 1
allele count: 12
allele frequency: 2.249297094657919e-4
allele num: 53350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.430A>G
  hgvsp: ENSP00000391430.2:p.Met144Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.482A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.443A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.449A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.430A>G
  hgvsp: ENSP00000363510.3:p.Met144Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.430A>G
  hgvsp: ENSP00000326261.8:p.Met144Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.437A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.127A>G
  hgvsp: ENSP00000441776.1:p.Met43Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.521A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.313A>G
  hgvsp: ENSP00000471084.1:p.Met105Val
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.582A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2533A>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000485441
  gene symbol: SRRM1
  hgvsc: ENST00000485441.1:n.8A>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30561
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met144Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

1-24976495-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976495
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976495
    reference: chr 1
allele count: 1
allele frequency: 1.810085798066828e-5
allele num: 55246
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.439C>G
  hgvsp: ENSP00000363510.3:p.Gln147Glu
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.136C>G
  hgvsp: ENSP00000441776.1:p.Gln46Glu
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.591C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.439C>G
  hgvsp: ENSP00000391430.2:p.Gln147Glu
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.458C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.439C>G
  hgvsp: ENSP00000326261.8:p.Gln147Glu
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.452C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.530C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2542C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000485441
  gene symbol: SRRM1
  hgvsc: ENST00000485441.1:n.17C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.322C>G
  hgvsp: ENSP00000471084.1:p.Gln108Glu
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.446C>G
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.491C>G
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln147Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

1-24976506-CAAAGAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24976506
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 24976500
    reference: chr 1
allele count: 1
allele frequency: 1.779739446145084e-5
allele num: 56188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000462710
  gene symbol: SRRM1
  hgvsc: ENST00000462710.1:n.2557_2562delGATAAA
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000441776
  ensembl transcript: ENST00000537199
  gene symbol: SRRM1
  hgvsc: ENST00000537199.1:c.151_156delGATAAA
  hgvsp: ENSP00000441776.1:p.Asp51_Lys52del
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000363510
  ensembl transcript: ENST00000374389
  gene symbol: SRRM1
  hgvsc: ENST00000374389.4:c.454_459delGATAAA
  hgvsp: ENSP00000363510.3:p.Asp152_Lys153del
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000478890
  gene symbol: SRRM1
  hgvsc: ENST00000478890.1:n.467_472delGATAAA
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000495561
  gene symbol: SRRM1
  hgvsc: ENST00000495561.1:n.461_466delGATAAA
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000468822
  gene symbol: SRRM1
  hgvsc: ENST00000468822.1:n.506_511delGATAAA
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000471084
  ensembl transcript: ENST00000596378
  gene symbol: SRRM1
  hgvsc: ENST00000596378.1:c.337_342delGATAAA
  hgvsp: ENSP00000471084.1:p.Asp113_Lys114del
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000490543
  gene symbol: SRRM1
  hgvsc: ENST00000490543.1:n.606_611delGATAAA
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000326261
  ensembl transcript: ENST00000323848
  gene symbol: SRRM1
  hgvsc: ENST00000323848.9:c.454_459delGATAAA
  hgvsp: ENSP00000326261.8:p.Asp152_Lys153del
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133226
  ensembl protein: ENSP00000391430
  ensembl transcript: ENST00000447431
  gene symbol: SRRM1
  hgvsc: ENST00000447431.2:c.454_459delGATAAA
  hgvsp: ENSP00000391430.2:p.Asp152_Lys153del
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000479034
  gene symbol: SRRM1
  hgvsc: ENST00000479034.1:n.473_478delGATAAA
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000494934
  gene symbol: SRRM1
  hgvsc: ENST00000494934.1:n.545_550delGATAAA
  variant of: http://identifiers.org/hgnc/16638
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133226
  ensembl transcript: ENST00000485441
  gene symbol: SRRM1
  hgvsc: ENST00000485441.1:n.32_37delGATAAA
  variant of: http://identifiers.org/hgnc/16638
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp152_Lys153del
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: CAAAGAT
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

GenotypeDepth
all individuals: 2172
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 805
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1575
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4894
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4275
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3588
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3517
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11567
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25480
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4251
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3006
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
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: 66652
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.15e-1

FS
type: SiteQuality
SIO_000300: 3.346e0

VQSLOD
type: SiteQuality
SIO_000300: -2.368e0

QD
type: SiteQuality
SIO_000300: 1.341e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.822341e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeDepth
all individuals: 6617
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1575
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2172
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3512
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11571
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4275
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4893
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4251
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3588
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3005
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25480
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.38e-1

DP
type: SiteQuality
SIO_000300: 2.822546e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.207e1

MQRankSum
type: SiteQuality
SIO_000300: -1.321e0

VQSLOD
type: SiteQuality
SIO_000300: -1.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.209e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

GenotypeDepth
all individuals: 805
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1575
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3004
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4872
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4247
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4270
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11179
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25480
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3005
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 338
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3587
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3505
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16284
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.55e-1

QD
type: SiteQuality
SIO_000300: 1.829e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 4.277e0

VQSLOD
type: SiteQuality
SIO_000300: -5.256999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.818682e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.606e0

GenotypeDepth
all individuals: 1576
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6618
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7729
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10444
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 145
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4236
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4266
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4807
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3487
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25481
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3002
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3587
bin: 9.25e1
variant carriers: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
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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
allele num: 10394
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.810619e6

MQ
type: SiteQuality
SIO_000300: 5.914e1

ReadPosRankSum
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SIO_000300: 9.75e-1

MQRankSum
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SIO_000300: -9.429999999999999e-1

VQSLOD
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: -3.844e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
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SIO_000300: 9.32e0

ClippingRankSum
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SIO_000300: -4.18e-1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

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

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

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

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

Latino
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allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.526115687516973e-5
allele num: 66282
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: -3.0e-4

ClippingRankSum
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SIO_000300: -5.07e-1

VQSLOD
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ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -2.821e0

FS
type: SiteQuality
SIO_000300: 5.639999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.07e-1

QD
type: SiteQuality
SIO_000300: 1.27e1

DP
type: SiteQuality
SIO_000300: 2.792764e6

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
all individuals: 8219
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variant carriers: 0

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

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

European (Finnish)
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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: 15298
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.53035336756267e-5
allele num: 66220
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.195e0

VQSLOD
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SIO_000300: 2.55e0

MQRankSum
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SIO_000300: 5.08e-1

ClippingRankSum
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SIO_000300: 3.9e-2

BaseQRankSum
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SIO_000300: 4.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.501e1

DP
type: SiteQuality
SIO_000300: 2.78418e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3464
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511121856866538e-5
allele num: 66176
num of homozygotes: 0

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

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

African
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allele count: 3
allele frequency: 2.894076789504148e-4
allele num: 10366
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQ
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SIO_000300: 5.943e1

FS
type: SiteQuality
SIO_000300: 2.747e0

ClippingRankSum
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SIO_000300: -2.23e-1

VQSLOD
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SIO_000300: 8.35e-1

BaseQRankSum
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SIO_000300: 3.56e0

DP
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SIO_000300: 2.779898e6

QD
type: SiteQuality
SIO_000300: 1.267e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.19e-1

GenotypeDepth
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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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: 15022
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.656509695290859e-5
allele num: 11552
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.512172992590352e-5
allele num: 66130
num of homozygotes: 0

Other
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num of homozygotes: 0

East Asian
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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FS
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQ
type: SiteQuality
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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

African
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allele count: 1
allele frequency: 9.66183574879227e-5
allele num: 10350
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

Other
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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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DP
type: SiteQuality
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MQRankSum
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FS
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BaseQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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QD
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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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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14096
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65852
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

African
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allele frequency: 1.938360147315371e-4
allele num: 10318
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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SIO_000300: -2.37e-1

VQSLOD
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DP
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InbreedingCoeff
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BaseQRankSum
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MQ
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FS
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QD
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ClippingRankSum
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SIO_000300: 2.18e0

ReadPosRankSum
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SIO_000300: 1.02e0

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

Other
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allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

East 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
allele num: 6614
num of homozygotes: 0

African
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allele frequency: 9.703085581214826e-5
allele num: 10306
num of homozygotes: 0

South 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 frequency: 0.0e0
allele num: 65810
num of homozygotes: 0

Latino
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num of homozygotes: 0

VQSLOD
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ReadPosRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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MQRankSum
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QD
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DP
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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

African
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allele frequency: 0.0e0
allele num: 584
num of homozygotes: 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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num of homozygotes: 0

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

ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ClippingRankSum
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QD
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MQ
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BaseQRankSum
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DP
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SIO_000300: 7.9953e4

FS
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SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

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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bin: 9.75e1
variant carriers: 2

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.020691738408095e-5
allele num: 66210
num of homozygotes: 0

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

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

Other
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.24e-1

VQSLOD
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MQRankSum
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FS
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InbreedingCoeff
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DP
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BaseQRankSum
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MQ
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ReadPosRankSum
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QD
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66210
num of homozygotes: 0

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

Other
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South Asian
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African
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allele frequency: 2.10252302763316e-3
allele num: 9988
num of homozygotes: 0

FS
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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QD
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MQ
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InbreedingCoeff
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SIO_000300: 7.2e-3

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele frequency: 1.159554730983302e-4
allele num: 8624
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African
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South Asian
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Other
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European (Finnish)
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num of homozygotes: 0

European (Non-Finnish)
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QD
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ClippingRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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DP
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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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num of homozygotes: 0

European (Non-Finnish)
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Latino
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South Asian
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Other
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East Asian
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African
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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ClippingRankSum
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DP
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VQSLOD
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InbreedingCoeff
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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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East Asian
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allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

Latino
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allele num: 11570
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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African
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allele num: 10066
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South Asian
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Other
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MQ
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SIO_000300: 5.96e1

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

Other
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East Asian
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African
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South Asian
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VQSLOD
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DP
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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FS
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QD
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ReadPosRankSum
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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

African
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European (Non-Finnish)
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Latino
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European (Finnish)
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East Asian
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South Asian
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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MQ
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FS
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MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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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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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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European (Finnish)
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FS
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VQSLOD
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InbreedingCoeff
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QD
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BaseQRankSum
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DP
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MQ
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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South Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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MQ
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ClippingRankSum
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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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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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10364
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 (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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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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QD
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FS
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DP
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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SIO_000300: -5.2e-2

GenotypeDepth
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variant carriers: 0

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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bin: 6.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
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

African
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allele count: 2
allele frequency: 1.931247585940518e-4
allele num: 10356
num of homozygotes: 0

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

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

Other
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South Asian
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allele frequency: 0.0e0
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DP
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SIO_000300: 2.262482e6

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

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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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

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

South Asian
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allele 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

East Asian
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allele count: 1
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QD
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MQRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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FS
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DP
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 3

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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East Asian
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num of homozygotes: 0

Other
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 66690
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African
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Latino
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allele num: 11572
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InbreedingCoeff
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VQSLOD
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FS
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MQ
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QD
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ClippingRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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GenotypeDepth
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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 (Non-Finnish)
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allele num: 66690
num of homozygotes: 0

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

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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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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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East Asian
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Other
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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: 1.501817198810561e-5
allele num: 66586
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 6.46e0

InbreedingCoeff
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VQSLOD
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FS
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QD
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MQ
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MQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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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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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 66554
num of homozygotes: 0

South Asian
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East Asian
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Latino
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MQ
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InbreedingCoeff
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VQSLOD
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FS
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QD
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BaseQRankSum
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DP
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ReadPosRankSum
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MQRankSum
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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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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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allele frequency: 1.213739531496541e-4
allele num: 16478
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

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

Other
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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
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BaseQRankSum
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SIO_000300: -4.584e0

MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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SIO_000300: -6.03e-1

ReadPosRankSum
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QD
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SIO_000300: 9.57e0

DP
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SIO_000300: 2.255136e6

GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510117789187557e-5
allele num: 66220
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

South Asian
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East 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 count: 0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 1.61e0

ClippingRankSum
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FS
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QD
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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DP
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BaseQRankSum
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GenotypeDepth
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variant carriers: 1

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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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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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

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

Latino
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allele frequency: 2.612785229054172e-4
allele num: 11482
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.55055668476777e-5
allele num: 65926
num of homozygotes: 0

East Asian
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MQRankSum
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 1.169864295741694e-4
allele num: 8548
num of homozygotes: 0

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

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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South Asian
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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

African
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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

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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BaseQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

DP
type: SiteQuality
SIO_000300: 2.230947e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 2.47e0

InbreedingCoeff
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SIO_000300: 2.4e-3

MQRankSum
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SIO_000300: -1.532e0

ClippingRankSum
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SIO_000300: -3.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.17e-1

MQ
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SIO_000300: 5.239e1

QD
type: SiteQuality
SIO_000300: 6.9e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.173708920187793e-4
allele num: 8520
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

FS
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MQ
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SIO_000300: 6.0e1

MQRankSum
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QD
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -2.46e-1

DP
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SIO_000300: 2.227705e6

ReadPosRankSum
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SIO_000300: 8.94e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.521051350693599e-5
allele num: 65744
num of homozygotes: 0

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.42e-1

QD
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SIO_000300: 1.818e1

ReadPosRankSum
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SIO_000300: -3.5e-2

MQ
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SIO_000300: 5.98e1

FS
type: SiteQuality
SIO_000300: 1.526e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

BaseQRankSum
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SIO_000300: 5.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.837e-1

DP
type: SiteQuality
SIO_000300: 2.227516e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5220700152207e-5
allele num: 65700
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.64e-1

FS
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SIO_000300: 0.0e0

QD
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SIO_000300: 1.633e1

BaseQRankSum
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SIO_000300: 5.61e0

MQ
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SIO_000300: 5.979e1

VQSLOD
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SIO_000300: 2.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 2.225228e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522487134983709e-5
allele num: 65682
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

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

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

MQRankSum
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SIO_000300: -8.179999999999999e-1

ClippingRankSum
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ReadPosRankSum
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DP
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MQ
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SIO_000300: 5.919e1

BaseQRankSum
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VQSLOD
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FS
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SIO_000300: 1.73e0

InbreedingCoeff
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SIO_000300: 1.4e-3

QD
type: SiteQuality
SIO_000300: 1.419e1

GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9646
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65498
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.177301624676242e-4
allele num: 8494
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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FS
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QD
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DP
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SIO_000300: 2.214457e6

GenotypeDepth
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variant carriers: 0

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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South Asian
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allele count: 1
allele frequency: 6.093102607847916e-5
allele num: 16412
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65370
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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ClippingRankSum
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FS
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MQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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QD
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ReadPosRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 1

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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.297160709363227e-4
allele num: 65298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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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 count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

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

South Asian
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allele count: 0
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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

InbreedingCoeff
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SIO_000300: 8.200000000000001e-3

QD
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FS
type: SiteQuality
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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SIO_000300: 4.6e-1

MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.205823e6

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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bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 3.065322012077369e-5
allele num: 65246
num of homozygotes: 0

East Asian
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allele frequency: 1.180080245456691e-4
allele num: 8474
num of homozygotes: 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: 1.515610791148833e-4
allele num: 6598
num of homozygotes: 0

Latino
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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 frequency: 0.0e0
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VQSLOD
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QD
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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SIO_000300: 1.02e0

MQRankSum
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SIO_000300: 2.26e-1

InbreedingCoeff
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SIO_000300: 3.8e-3

GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

South Asian
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allele frequency: 0.0e0
allele num: 16408
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 frequency: 1.532661006038684e-5
allele num: 65246
num of homozygotes: 0

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

Other
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allele num: 888
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

ReadPosRankSum
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DP
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MQ
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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SIO_000300: 3.8e-3

BaseQRankSum
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QD
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SIO_000300: 1.503e1

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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bin: 6.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64534
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.084128360797918e-4
allele num: 9224
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.186195e6

VQSLOD
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SIO_000300: -3.802e-1

ClippingRankSum
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SIO_000300: 4.41e-1

BaseQRankSum
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FS
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SIO_000300: 0.0e0

QD
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MQRankSum
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ReadPosRankSum
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SIO_000300: -8.1e-2

MQ
type: SiteQuality
SIO_000300: 5.871e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

GenotypeDepth
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variant carriers: 0

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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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
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allele count: 1
allele frequency: 1.549474728067185e-5
allele num: 64538
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele num: 9200
num of homozygotes: 0

European (Finnish)
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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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num of homozygotes: 0

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

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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variant carriers: 2

South Asian
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allele frequency: 0.0e0
allele num: 4096
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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Latino
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Other
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African
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allele num: 4028
num of homozygotes: 0

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

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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num of homozygotes: 0

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

Other
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South Asian
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African
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East Asian
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European (Finnish)
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FS
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VQSLOD
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MQ
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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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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European (Non-Finnish)
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allele num: 14366
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European (Finnish)
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Other
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South Asian
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Latino
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East Asian
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African
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ReadPosRankSum
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FS
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MQ
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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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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African
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European (Finnish)
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South Asian
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Other
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East Asian
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European (Non-Finnish)
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ClippingRankSum
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MQ
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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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BaseQRankSum
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ReadPosRankSum
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QD
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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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num of homozygotes: 0

South Asian
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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 num: 14644
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Latino
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VQSLOD
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DP
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BaseQRankSum
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QD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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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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Latino
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allele frequency: 9.803921568627451e-4
allele num: 1020
num of homozygotes: 0

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

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

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

GenotypeQuality
all individuals: 884
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30734
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2950
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16043
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3898
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.499685028347449e-5
allele num: 28574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9888
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 446
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

QD
type: SiteQuality
SIO_000300: 3.23e0

MQ
type: SiteQuality
SIO_000300: 5.767e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

DP
type: SiteQuality
SIO_000300: 1.035051e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0