14-73554661-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554661
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554661
    reference: chr 14
allele count: 1
allele frequency: 8.587819037477242e-6
allele num: 116444
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.383-48T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.383-48T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.562-48T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.383-48T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.383-48T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.383-48T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.383-48T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.325-48T>C
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1899
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3318
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4741
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1392
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3043
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2114
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ

14-73554669-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554669
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554669
    reference: chr 14
allele count: 1
allele frequency: 8.550662676357418e-6
allele num: 116950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.383-40G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.383-40G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.383-40G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.325-40G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.383-40G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.383-40G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.383-40G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.562-40G>A
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25322
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2345
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2142
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8443
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2004
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

14-73554676-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554676
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554676
    reference: chr 14
allele count: 3
allele frequency: 2.542717656631408e-5
allele num: 117984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.383-33G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.383-33G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.383-33G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.325-33G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.383-33G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.562-33G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.383-33G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.383-33G>T
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11811
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7289
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1680
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1241
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

14-73554679-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554679
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554679
    reference: chr 14
allele count: 1
allele frequency: 8.443806467955754e-6
allele num: 118430
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.325-30A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.383-30A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.383-30A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.383-30A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.383-30A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.383-30A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.562-30A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.383-30A>G
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12128
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1473
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3057
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-73554681-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554681
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554681
    reference: chr 14
allele count: 1
allele frequency: 8.421761832575375e-6
allele num: 118740
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.383-28T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.383-28T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.383-28T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.325-28T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.383-28T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.383-28T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.383-28T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.562-28T>G
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25719
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7578
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2191
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

14-73554699-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554699
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554699
    reference: chr 14
allele count: 1
allele frequency: 8.285965232089886e-6
allele num: 120686
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.383-10C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.383-10C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.383-10C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.383-10C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.383-10C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.383-10C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.562-10C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.325-10C>T
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7937
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3203
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ

14-73554705-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554705
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554705
    reference: chr 14
allele count: 1
allele frequency: 8.26405302216419e-6
allele num: 121006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.383-4C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.383-4C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.325-4C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.383-4C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.383-4C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.383-4C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.383-4C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.562-4C>T
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13247
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: c.383-4C>T
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

14-73554713-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554713
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554713
    reference: chr 14
allele count: 2
allele frequency: 1.649892756970797e-5
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.387C>T
  hgvsp: ENST00000526754.1:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.387C>T
  hgvsp: ENST00000525321.1:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.329C>T
  hgvsp: ENSP00000434444.1:p.Ser110Leu
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.387C>T
  hgvsp: ENST00000527432.1:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.387C>T
  hgvsp: ENST00000531500.1:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.387C>T
  hgvsp: ENST00000261973.7:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.566C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.387C>T
  hgvsp: ENST00000540173.1:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8053
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser110Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

14-73554728-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554728
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554728
    reference: chr 14
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.402C>T
  hgvsp: ENST00000527432.1:c.402C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.344C>T
  hgvsp: ENSP00000434444.1:p.Thr115Ile
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.402C>T
  hgvsp: ENST00000525321.1:c.402C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.402C>T
  hgvsp: ENST00000526754.1:c.402C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.581C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.402C>T
  hgvsp: ENST00000540173.1:c.402C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.402C>T
  hgvsp: ENST00000261973.7:c.402C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.402C>T
  hgvsp: ENST00000531500.1:c.402C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7305
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2297
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3256
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr115Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

14-73554730-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554730
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554730
    reference: chr 14
allele count: 2
allele frequency: 1.648179585647652e-5
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.404A>G
  hgvsp: ENSP00000434333.1:p.Lys135Arg
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.404A>G
  hgvsp: ENSP00000261973.7:p.Lys135Arg
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.346A>G
  hgvsp: ENSP00000434444.1:p.Arg116Gly
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.404A>G
  hgvsp: ENSP00000436868.1:p.Lys135Arg
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.404A>G
  hgvsp: ENSP00000437934.1:p.Lys135Arg
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.404A>G
  hgvsp: ENSP00000436225.1:p.Lys135Arg
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.404A>G
  hgvsp: ENSP00000431150.1:p.Lys135Arg
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.583A>G
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1671
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27963
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8087
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2298
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys135Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

14-73554734-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554734
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554734
    reference: chr 14
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.408G>A
  hgvsp: ENST00000531500.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.408G>A
  hgvsp: ENST00000525321.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.587G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.408G>A
  hgvsp: ENST00000527432.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.408G>A
  hgvsp: ENST00000261973.7:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.350G>A
  hgvsp: ENSP00000434444.1:p.Ser117Asn
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.408G>A
  hgvsp: ENST00000526754.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.408G>A
  hgvsp: ENST00000540173.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8672
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8090
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser117Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum

14-73554740-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554740
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554740
    reference: chr 14
allele count: 32
allele frequency: 2.636348657109903e-4
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.414A>G
  hgvsp: ENST00000261973.7:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.414A>G
  hgvsp: ENST00000527432.1:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.593A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.356A>G
  hgvsp: ENSP00000434444.1:p.Asn119Ser
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.414A>G
  hgvsp: ENST00000526754.1:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.414A>G
  hgvsp: ENST00000531500.1:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.414A>G
  hgvsp: ENST00000525321.1:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.414A>G
  hgvsp: ENST00000540173.1:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 31123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27971
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asn119Ser
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

14-73554746-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554746
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554746
    reference: chr 14
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.420C>G
  hgvsp: ENST00000527432.1:c.420C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.420C>G
  hgvsp: ENST00000261973.7:c.420C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.420C>G
  hgvsp: ENST00000526754.1:c.420C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.362C>G
  hgvsp: ENSP00000434444.1:p.Pro121Arg
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.420C>G
  hgvsp: ENST00000540173.1:c.420C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.420C>G
  hgvsp: ENST00000531500.1:c.420C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.420C>G
  hgvsp: ENST00000525321.1:c.420C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.599C>G
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8101
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro121Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

14-73554749-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554749
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554749
    reference: chr 14
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.423C>T
  hgvsp: ENST00000526754.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.423C>T
  hgvsp: ENST00000261973.7:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.423C>T
  hgvsp: ENST00000525321.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.423C>T
  hgvsp: ENST00000540173.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.423C>T
  hgvsp: ENST00000527432.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.365C>T
  hgvsp: ENSP00000434444.1:p.Ser122Phe
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.423C>T
  hgvsp: ENST00000531500.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.602C>T
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31077
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3841
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2296
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser122Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

http://identifiers.org/exac.variant/14-73554755-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554755
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554755
    reference: chr 14
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.429A>C
  hgvsp: ENST00000525321.1:c.429A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.429A>C
  hgvsp: ENST00000531500.1:c.429A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.429A>C
  hgvsp: ENST00000526754.1:c.429A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.429A>C
  hgvsp: ENST00000261973.7:c.429A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.429A>C
  hgvsp: ENST00000527432.1:c.429A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.429A>C
  hgvsp: ENST00000540173.1:c.429A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.371A>C
  hgvsp: ENSP00000434444.1:p.His124Pro
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.608A>C
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4824
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8103
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.His124Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS

14-73554755-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554755
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554755
    reference: chr 14
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.429A>G
  hgvsp: ENST00000525321.1:c.429A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.371A>G
  hgvsp: ENSP00000434444.1:p.His124Arg
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.608A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.429A>G
  hgvsp: ENST00000261973.7:c.429A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.429A>G
  hgvsp: ENST00000527432.1:c.429A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.429A>G
  hgvsp: ENST00000540173.1:c.429A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.429A>G
  hgvsp: ENST00000531500.1:c.429A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.429A>G
  hgvsp: ENST00000526754.1:c.429A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8103
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4824
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His124Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

14-73554762-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554762
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554762
    reference: chr 14
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.436T>C
  hgvsp: ENST00000525321.1:c.436T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.436T>C
  hgvsp: ENST00000526754.1:c.436T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.436T>C
  hgvsp: ENST00000527432.1:c.436T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.378T>C
  hgvsp: ENST00000528081.1:c.378T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.436T>C
  hgvsp: ENST00000531500.1:c.436T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.615T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.436T>C
  hgvsp: ENST00000261973.7:c.436T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.436T>C
  hgvsp: ENST00000540173.1:c.436T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3271
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8704
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu146Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

14-73554797-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554797
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554797
    reference: chr 14
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.471A>G
  hgvsp: ENST00000527432.1:c.471A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.471A>G
  hgvsp: ENST00000526754.1:c.471A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.471A>G
  hgvsp: ENST00000261973.7:c.471A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.650A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.471A>G
  hgvsp: ENST00000531500.1:c.471A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.471A>G
  hgvsp: ENST00000525321.1:c.471A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.471A>G
  hgvsp: ENST00000540173.1:c.471A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.413A>G
  hgvsp: ENSP00000434444.1:p.Tyr138Cys
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7366
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3844
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr138Cys
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

14-73554815-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554815
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554815
    reference: chr 14
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.489A>G
  hgvsp: ENST00000531500.1:c.489A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.489A>G
  hgvsp: ENST00000261973.7:c.489A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.489A>G
  hgvsp: ENST00000525321.1:c.489A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.489A>G
  hgvsp: ENST00000540173.1:c.489A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.431A>G
  hgvsp: ENSP00000434444.1:p.Gln144Arg
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.489A>G
  hgvsp: ENST00000527432.1:c.489A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.668A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.489A>G
  hgvsp: ENST00000526754.1:c.489A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27940
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln144Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

14-73554818-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554818
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554818
    reference: chr 14
allele count: 5
allele frequency: 4.11834475487612e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.492G>A
  hgvsp: ENST00000540173.1:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.492G>A
  hgvsp: ENST00000261973.7:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.434G>A
  hgvsp: ENSP00000434444.1:p.Arg145Lys
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.492G>A
  hgvsp: ENST00000531500.1:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.492G>A
  hgvsp: ENST00000526754.1:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.492G>A
  hgvsp: ENST00000527432.1:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.671G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.492G>A
  hgvsp: ENST00000525321.1:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8112
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8711
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg145Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

14-73554825-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554825
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554825
    reference: chr 14
allele count: 7
allele frequency: 5.765682656826568e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.499G>T
  hgvsp: ENSP00000437934.1:p.Ala167Ser
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.499G>T
  hgvsp: ENSP00000436225.1:p.Ala167Ser
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.499G>T
  hgvsp: ENSP00000261973.7:p.Ala167Ser
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.678G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.499G>T
  hgvsp: ENSP00000436868.1:p.Ala167Ser
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.499G>T
  hgvsp: ENSP00000431150.1:p.Ala167Ser
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.441G>T
  hgvsp: ENSP00000434444.1:p.Arg147Ser
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.499G>T
  hgvsp: ENSP00000434333.1:p.Ala167Ser
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala167Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

14-73554826-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554826
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554826
    reference: chr 14
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.679C>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.500C>G
  hgvsp: ENSP00000261973.7:p.Ala167Gly
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.500C>G
  hgvsp: ENSP00000434333.1:p.Ala167Gly
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.500C>G
  hgvsp: ENSP00000431150.1:p.Ala167Gly
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.500C>G
  hgvsp: ENSP00000436868.1:p.Ala167Gly
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.500C>G
  hgvsp: ENSP00000437934.1:p.Ala167Gly
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.442C>G
  hgvsp: ENSP00000434444.1:p.His148Asp
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.500C>G
  hgvsp: ENSP00000436225.1:p.Ala167Gly
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4834
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8111
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8716
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala167Gly
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

14-73554827-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554827
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554827
    reference: chr 14
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.501A>G
  hgvsp: ENST00000526754.1:c.501A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.443A>G
  hgvsp: ENSP00000434444.1:p.His148Arg
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.501A>G
  hgvsp: ENST00000531500.1:c.501A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.501A>G
  hgvsp: ENST00000525321.1:c.501A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.501A>G
  hgvsp: ENST00000261973.7:c.501A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.501A>G
  hgvsp: ENST00000527432.1:c.501A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.501A>G
  hgvsp: ENST00000540173.1:c.501A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.680A>G
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8718
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His148Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

14-73554831-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554831
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554831
    reference: chr 14
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.505C>T
  hgvsp: ENST00000540173.1:c.505C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.684C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.505C>T
  hgvsp: ENST00000527432.1:c.505C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.505C>T
  hgvsp: ENST00000261973.7:c.505C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.505C>T
  hgvsp: ENST00000531500.1:c.505C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.505C>T
  hgvsp: ENST00000526754.1:c.505C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.505C>T
  hgvsp: ENST00000525321.1:c.505C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.447C>T
  hgvsp: ENST00000528081.1:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4836
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8718
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3844
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu169Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP

14-73554861-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554861
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554861
    reference: chr 14
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.535T>G
  hgvsp: ENSP00000436868.1:p.Ser179Ala
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.714T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.477T>G
  hgvsp: ENST00000528081.1:c.477T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.535T>G
  hgvsp: ENSP00000434333.1:p.Ser179Ala
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.535T>G
  hgvsp: ENSP00000436225.1:p.Ser179Ala
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.535T>G
  hgvsp: ENSP00000431150.1:p.Ser179Ala
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.535T>G
  hgvsp: ENSP00000437934.1:p.Ser179Ala
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.535T>G
  hgvsp: ENSP00000261973.7:p.Ser179Ala
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8719
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2306
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27807
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser179Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ

14-73554866-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554866
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554866
    reference: chr 14
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.482T>C
  hgvsp: ENSP00000434444.1:p.Met161Thr
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.540T>C
  hgvsp: ENST00000526754.1:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.540T>C
  hgvsp: ENST00000525321.1:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.540T>C
  hgvsp: ENST00000261973.7:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.540T>C
  hgvsp: ENST00000527432.1:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.540T>C
  hgvsp: ENST00000531500.1:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.540T>C
  hgvsp: ENST00000540173.1:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.719T>C
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4834
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2306
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Met161Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

14-73554868-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554868
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554868
    reference: chr 14
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.542G>T
  hgvsp: ENSP00000434333.1:p.Gly181Val
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.484G>T
  hgvsp: ENSP00000434444.1:p.Gly162Trp
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.542G>T
  hgvsp: ENSP00000261973.7:p.Gly181Val
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.542G>T
  hgvsp: ENSP00000436868.1:p.Gly181Val
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.721G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.542G>T
  hgvsp: ENSP00000437934.1:p.Gly181Val
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.542G>T
  hgvsp: ENSP00000431150.1:p.Gly181Val
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.542G>T
  hgvsp: ENSP00000436225.1:p.Gly181Val
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3273
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly181Val
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

14-73554872-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554872
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554872
    reference: chr 14
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+3A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+3A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+3A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+3A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+3A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+3A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.485+3A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+3A>G
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4833
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27615
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2306
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
hgvs: c.543+3A>G
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

14-73554878-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554878
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554878
    reference: chr 14
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+9T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+9T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+9T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+9T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+9T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+9T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+9T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.485+9T>C
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30474
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-73554880-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554880
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554880
    reference: chr 14
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+11T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+11T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+11T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+11T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+11T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+11T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.485+11T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+11T>G
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8045
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3268
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3841
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4827
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD

14-73554883-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554883
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554883
    reference: chr 14
allele count: 2
allele frequency: 1.649076517150396e-5
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+14C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+14C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+14C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+14C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+14C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+14C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+14C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.485+14C>T
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27074
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1682
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

14-73554884-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554884
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554884
    reference: chr 14
allele count: 81
allele frequency: 6.679200474965367e-4
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+15G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.485+15G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+15G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+15G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+15G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+15G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+15G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+15G>A
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 13534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3835
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8017
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3262
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

14-73554886-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554886
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554886
    reference: chr 14
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.485+17G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+17G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+17G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+17G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+17G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+17G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+17G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+17G>A
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1682
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8013
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3261
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

14-73554890-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554890
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554890
    reference: chr 14
allele count: 11127
allele frequency: 9.178269763758744e-2
allele num: 121232
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+21T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+21T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.485+21T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+21T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+21T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+21T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+21T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+21T>C
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 3.75e1
  variant carriers: 249
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.25e1
  variant carriers: 685
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 661
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 5.25e1
  variant carriers: 354
genotype depth: GenotypeDepth
  all individuals: 11320
  bin: 2.75e1
  variant carriers: 185
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.25e1
  variant carriers: 570
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 4.25e1
  variant carriers: 280
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 6.75e1
  variant carriers: 674
genotype depth: GenotypeDepth
  all individuals: 24812
  bin: 2.25e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 5.75e1
  variant carriers: 484
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 8.25e1
  variant carriers: 718
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 3.25e1
  variant carriers: 217
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 322
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 8.75e1
  variant carriers: 767
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 7.75e1
  variant carriers: 762
genotype depth: GenotypeDepth
  all individuals: 4034
  bin: 9.75e1
  variant carriers: 3369
genotype quality: GenotypeQuality
  all individuals: 3897
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 624
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

14-73554894-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554894
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554894
    reference: chr 14
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+25T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+25T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+25T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+25T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+25T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+25T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+25T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.485+25T>G
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14443
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2878
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

14-73554906-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554906
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554904
    reference: chr 14
allele count: 3
allele frequency: 2.476555276713776e-5
allele num: 121136
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+40_543+41delTG
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+40_543+41delTG
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+40_543+41delTG
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+40_543+41delTG
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+40_543+41delTG
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.485+40_485+41delTG
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+40_722+41delTG
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+40_543+41delTG
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4271
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6903
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1632
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: CTG
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

14-73554907-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554907
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554907
    reference: chr 14
allele count: 4
allele frequency: 3.302073702285035e-5
allele num: 121136
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+38T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+38T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+38T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+38T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+38T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+38T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.485+38T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+38T>C
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4277
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2864
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2399
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS

14-73554908-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554908
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554908
    reference: chr 14
allele count: 4
allele frequency: 3.302618976848641e-5
allele num: 121116
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+39G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+39G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+39G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+39G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+39G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.485+39G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+39G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+39G>A
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14446
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2399
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

14-73554913-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73554913
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73554913
    reference: chr 14
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+44A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+44A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+44A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+44A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.485+44A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+44A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+44A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+44A>G
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20504
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6832
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

14-73555030-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73555030
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73555030
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 23464
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.486-48T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+161T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+161T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+161T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+161T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+161T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+161T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+161T>A
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 30341
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12559
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3192
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-73555056-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73555056
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73555056
    reference: chr 14
allele count: 1
allele frequency: 6.584145377929945e-5
allele num: 15188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+187A>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+187A>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+187A>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.486-22A>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+187A>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+187A>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+187A>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+187A>C
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2244
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30670
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 971
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD

14-73555069-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73555069
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73555069
    reference: chr 14
allele count: 64
allele frequency: 4.587813620071685e-3
allele num: 13950
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+200T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+200T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+200T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+200T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+200T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+200T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+200T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.486-9T>A
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27899
  bin: 2.5e0
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 7.5e0
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25469
  bin: 7.5e0
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 8.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2871
  bin: 2.5e0
  variant carriers: 2
num of homozygotes: 1
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD

14-73555070-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73555070
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73555070
    reference: chr 14
allele count: 1
allele frequency: 7.189072609633358e-5
allele num: 13910
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+201T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+201T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.486-8T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+201T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+201T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+201T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+201T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+201T>C
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25916
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2669
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
hgvs: c.486-8T>C
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-73555084-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73555084
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73555084
    reference: chr 14
allele count: 1
allele frequency: 7.453786523553965e-5
allele num: 13416
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+215A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+215A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.492A>G
  hgvsp: ENST00000528081.1:c.492A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+215A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+215A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+215A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+215A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+215A>G
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2149
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2400
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly164Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum

14-73555088-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73555088
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73555088
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 13318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*1A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+219A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+219A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+219A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+219A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+219A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+219A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+219A>G
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24040
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2587
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21700
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

14-73555106-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73555106
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73555106
    reference: chr 14
allele count: 24
allele frequency: 1.892147587511826e-3
allele num: 12684
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.543+237G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*19G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.543+237G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.543+237G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.543+237G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.543+237G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.722+237G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.543+237G>A
  variant of: http://identifiers.org/hgnc/23244
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20073
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3966
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

14-73563573-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563573
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563573
    reference: chr 14
allele count: 9
allele frequency: 7.670933978828223e-5
allele num: 117326
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.544-50G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.544-50G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.544-50G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.544-50G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.544-50G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.723-50G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*96-50G>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.544-50G>T
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15050
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10732
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6365
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13589
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4405
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4254
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1195
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2368
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5709
  bin: 9.75e1
  variant carriers: 10
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

14-73563581-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563581
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563581
    reference: chr 14
allele count: 1
allele frequency: 8.475869200386499e-6
allele num: 117982
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.544-42T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.544-42T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.544-42T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.544-42T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.544-42T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.544-42T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*96-42T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.723-42T>G
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2170
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5706
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6670
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2741
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

14-73563598-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563598
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563598
    reference: chr 14
allele count: 1
allele frequency: 8.376752835530836e-6
allele num: 119378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*96-25C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.544-25C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.544-25C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.723-25C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.544-25C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.544-25C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.544-25C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.544-25C>T
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1238
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

14-73563599-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563599
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563599
    reference: chr 14
allele count: 2
allele frequency: 1.673360107095047e-5
allele num: 119520
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.544-24C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*96-24C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.544-24C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.544-24C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.544-24C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.544-24C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.544-24C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.723-24C>T
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2730
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34394
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2133
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

14-73563601-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563601
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563601
    reference: chr 14
allele count: 1
allele frequency: 8.353381448810478e-6
allele num: 119712
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.544-22T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.544-22T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*96-22T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.544-22T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.544-22T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.544-22T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.723-22T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.544-22T>C
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7276
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-73563606-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563606
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563606
    reference: chr 14
allele count: 2
allele frequency: 1.663395322532353e-5
allele num: 120236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.544-17T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.544-17T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.544-17T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.723-17T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*96-17T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.544-17T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.544-17T>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.544-17T>G
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

14-73563606-TTGCTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563606
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563601
    reference: chr 14
allele count: 1
allele frequency: 8.316976612661764e-6
allele num: 120236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.544-15_544-11delGCTGT
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.544-15_544-11delGCTGT
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.544-15_544-11delGCTGT
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.544-15_544-11delGCTGT
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.544-15_544-11delGCTGT
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.723-15_723-11delGCTGT
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.544-15_544-11delGCTGT
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*96-15_*96-11delGCTGT
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35631
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: TTGCTG
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

14-73563615-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563615
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563615
    reference: chr 14
allele count: 1
allele frequency: 8.279790686891435e-6
allele num: 120776
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.544-8T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*96-8T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.544-8T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.544-8T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.544-8T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.544-8T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.544-8T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.723-8T>C
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
hgvs: c.544-8T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

14-73563616-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563616
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563616
    reference: chr 14
allele count: 86
allele frequency: 7.118733858684855e-4
allele num: 120808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.544-7G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*96-7G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.544-7G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.544-7G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.544-7G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.544-7G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.544-7G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.723-7G>A
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 28209
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16950
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 3.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36237
  bin: 6.25e1
  variant carriers: 0
hgvs: c.544-7G>A
num of homozygotes: 2
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

14-73563625-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563625
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563625
    reference: chr 14
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.546T>C
  hgvsp: ENST00000525321.1:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.546T>C
  hgvsp: ENST00000540173.1:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.546T>C
  hgvsp: ENST00000531500.1:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.546T>C
  hgvsp: ENST00000526754.1:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*98T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.546T>C
  hgvsp: ENST00000261973.7:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.725T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.546T>C
  hgvsp: ENST00000527432.1:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2156
  bin: 8.25e1
  variant carriers: 0
hgvs: c.546T>C
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

14-73563640-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563640
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563640
    reference: chr 14
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.561T>C
  hgvsp: ENST00000526754.1:c.561T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*113T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.561T>C
  hgvsp: ENST00000525321.1:c.561T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.561T>C
  hgvsp: ENST00000261973.7:c.561T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.740T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.561T>C
  hgvsp: ENST00000531500.1:c.561T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.561T>C
  hgvsp: ENST00000540173.1:c.561T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.561T>C
  hgvsp: ENST00000527432.1:c.561T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5702
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr187Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

14-73563643-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563643
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563643
    reference: chr 14
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.564C>G
  hgvsp: ENST00000531500.1:c.564C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.564C>G
  hgvsp: ENST00000526754.1:c.564C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.564C>G
  hgvsp: ENST00000527432.1:c.564C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.564C>G
  hgvsp: ENST00000261973.7:c.564C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.564C>G
  hgvsp: ENST00000540173.1:c.564C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.564C>G
  hgvsp: ENST00000525321.1:c.564C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.743C>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*116C>G
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val188Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-73563652-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563652
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563652
    reference: chr 14
allele count: 74
allele frequency: 6.100074190091502e-4
allele num: 121310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.573C>G
  hgvsp: ENSP00000437934.1:p.Asp191Glu
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.573C>G
  hgvsp: ENSP00000436868.1:p.Asp191Glu
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.573C>G
  hgvsp: ENSP00000431150.1:p.Asp191Glu
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.573C>G
  hgvsp: ENSP00000434333.1:p.Asp191Glu
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.752C>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.573C>G
  hgvsp: ENSP00000261973.7:p.Asp191Glu
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*125C>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.573C>G
  hgvsp: ENSP00000436225.1:p.Asp191Glu
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 28303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 17268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3410
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp191Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

14-73563652-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563652
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563652
    reference: chr 14
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.573C>T
  hgvsp: ENST00000261973.7:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.573C>T
  hgvsp: ENST00000531500.1:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.573C>T
  hgvsp: ENST00000525321.1:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*125C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.752C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.573C>T
  hgvsp: ENST00000526754.1:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.573C>T
  hgvsp: ENST00000527432.1:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.573C>T
  hgvsp: ENST00000540173.1:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7495
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5776
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp191Asp
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

14-73563653-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563653
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563653
    reference: chr 14
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.574G>A
  hgvsp: ENSP00000434333.1:p.Asp192Asn
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.574G>A
  hgvsp: ENSP00000437934.1:p.Asp192Asn
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.574G>A
  hgvsp: ENSP00000261973.7:p.Asp192Asn
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.574G>A
  hgvsp: ENSP00000436868.1:p.Asp192Asn
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.574G>A
  hgvsp: ENSP00000431150.1:p.Asp192Asn
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*126G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.574G>A
  hgvsp: ENSP00000436225.1:p.Asp192Asn
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.753G>A
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36825
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp192Asn
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-73563662-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563662
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563662
    reference: chr 14
allele count: 3
allele frequency: 2.472310126582278e-5
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.583G>A
  hgvsp: ENSP00000434333.1:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.583G>A
  hgvsp: ENSP00000436225.1:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.583G>A
  hgvsp: ENSP00000436868.1:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.583G>A
  hgvsp: ENSP00000261973.7:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*135G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.762G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.583G>A
  hgvsp: ENSP00000431150.1:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.583G>A
  hgvsp: ENSP00000437934.1:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala195Thr
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

14-73563664-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563664
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563664
    reference: chr 14
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.585C>G
  hgvsp: ENST00000526754.1:c.585C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.585C>G
  hgvsp: ENST00000525321.1:c.585C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.585C>G
  hgvsp: ENST00000261973.7:c.585C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.585C>G
  hgvsp: ENST00000531500.1:c.585C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*137C>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.585C>G
  hgvsp: ENST00000527432.1:c.585C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.585C>G
  hgvsp: ENST00000540173.1:c.585C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.764C>G
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36842
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7518
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2786
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala195Ala
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

14-73563707-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563707
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563707
    reference: chr 14
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.628G>A
  hgvsp: ENSP00000436868.1:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.807G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.628G>A
  hgvsp: ENSP00000437934.1:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*180G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.628G>A
  hgvsp: ENSP00000431150.1:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.628G>A
  hgvsp: ENSP00000434333.1:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.628G>A
  hgvsp: ENSP00000436225.1:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.628G>A
  hgvsp: ENSP00000261973.7:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2786
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36823
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala210Thr
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

14-73563709-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563709
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563709
    reference: chr 14
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.630T>A
  hgvsp: ENST00000527432.1:c.630T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.809T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.630T>A
  hgvsp: ENST00000540173.1:c.630T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.630T>A
  hgvsp: ENST00000526754.1:c.630T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.630T>A
  hgvsp: ENST00000261973.7:c.630T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.630T>A
  hgvsp: ENST00000525321.1:c.630T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*182T>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.630T>A
  hgvsp: ENST00000531500.1:c.630T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5704
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7517
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3412
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2786
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala210Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

14-73563710-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563710
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563710
    reference: chr 14
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.631A>G
  hgvsp: ENSP00000437934.1:p.Ile211Val
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*183A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.810A>G
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.631A>G
  hgvsp: ENSP00000431150.1:p.Ile211Val
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.631A>G
  hgvsp: ENSP00000436868.1:p.Ile211Val
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.631A>G
  hgvsp: ENSP00000434333.1:p.Ile211Val
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.631A>G
  hgvsp: ENSP00000436225.1:p.Ile211Val
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.631A>G
  hgvsp: ENSP00000261973.7:p.Ile211Val
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2785
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1248
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile211Val
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

14-73563754-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563754
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563754
    reference: chr 14
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.675C>T
  hgvsp: ENST00000527432.1:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.675C>T
  hgvsp: ENST00000540173.1:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.854C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.675C>T
  hgvsp: ENST00000525321.1:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*227C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.675C>T
  hgvsp: ENST00000261973.7:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434950
  ensembl transcript: ENST00000532192
  gene symbol: RBM25
  hgvsc: ENST00000532192.1:c.11C>T
  hgvsp: ENST00000532192.1:c.11C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.675C>T
  hgvsp: ENST00000526754.1:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.675C>T
  hgvsp: ENST00000531500.1:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro225Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

14-73563771-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563771
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563771
    reference: chr 14
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.692C>T
  hgvsp: ENSP00000436225.1:p.Ser231Phe
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.692C>T
  hgvsp: ENSP00000431150.1:p.Ser231Phe
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.871C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.692C>T
  hgvsp: ENSP00000436868.1:p.Ser231Phe
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.692C>T
  hgvsp: ENSP00000437934.1:p.Ser231Phe
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434950
  ensembl transcript: ENST00000532192
  gene symbol: RBM25
  hgvsc: ENST00000532192.1:c.28C>T
  hgvsp: ENSP00000434950.1:p.Ser10Phe
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*244C>T
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.692C>T
  hgvsp: ENSP00000261973.7:p.Ser231Phe
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.692C>T
  hgvsp: ENSP00000434333.1:p.Ser231Phe
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser231Phe
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

14-73563772-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563772
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563772
    reference: chr 14
allele count: 3
allele frequency: 2.477496077297878e-5
allele num: 121090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.693T>C
  hgvsp: ENST00000527432.1:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434950
  ensembl transcript: ENST00000532192
  gene symbol: RBM25
  hgvsc: ENST00000532192.1:c.29T>C
  hgvsp: ENST00000532192.1:c.29T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.872T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.693T>C
  hgvsp: ENST00000531500.1:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*245T>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.693T>C
  hgvsp: ENST00000540173.1:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.693T>C
  hgvsp: ENST00000526754.1:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.693T>C
  hgvsp: ENST00000525321.1:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.693T>C
  hgvsp: ENST00000261973.7:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5702
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser231Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

14-73563793-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563793
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563793
    reference: chr 14
allele count: 1
allele frequency: 8.296276631047985e-6
allele num: 120536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*266G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434950
  ensembl transcript: ENST00000532192
  gene symbol: RBM25
  hgvsc: ENST00000532192.1:c.50G>A
  hgvsp: ENST00000532192.1:c.50G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.893G>A
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.714G>A
  hgvsp: ENST00000540173.1:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.714G>A
  hgvsp: ENST00000526754.1:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.714G>A
  hgvsp: ENST00000527432.1:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.714G>A
  hgvsp: ENST00000261973.7:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.714G>A
  hgvsp: ENST00000525321.1:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.714G>A
  hgvsp: ENST00000531500.1:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys238Lys
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

14-73563805-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73563805
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 73563805
    reference: chr 14
allele count: 1
allele frequency: 8.36456102783726e-6
allele num: 119552
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000431150
  ensembl transcript: ENST00000527432
  gene symbol: RBM25
  hgvsc: ENST00000527432.1:c.726G>C
  hgvsp: ENSP00000431150.1:p.Glu242Asp
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434950
  ensembl transcript: ENST00000532192
  gene symbol: RBM25
  hgvsc: ENST00000532192.1:c.62G>C
  hgvsp: ENSP00000434950.1:p.Glu21Asp
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000261973
  ensembl transcript: ENST00000261973
  gene symbol: RBM25
  hgvsc: ENST00000261973.7:c.726G>C
  hgvsp: ENSP00000261973.7:p.Glu242Asp
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436225
  ensembl transcript: ENST00000526754
  gene symbol: RBM25
  hgvsc: ENST00000526754.1:c.726G>C
  hgvsp: ENSP00000436225.1:p.Glu242Asp
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000437934
  ensembl transcript: ENST00000540173
  gene symbol: RBM25
  hgvsc: ENST00000540173.1:c.726G>C
  hgvsp: ENSP00000437934.1:p.Glu242Asp
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119707
  ensembl transcript: ENST00000532683
  gene symbol: RBM25
  hgvsc: ENST00000532683.1:n.905G>C
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000436868
  ensembl transcript: ENST00000525321
  gene symbol: RBM25
  hgvsc: ENST00000525321.1:c.726G>C
  hgvsp: ENSP00000436868.1:p.Glu242Asp
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434333
  ensembl transcript: ENST00000531500
  gene symbol: RBM25
  hgvsc: ENST00000531500.1:c.726G>C
  hgvsp: ENSP00000434333.1:p.Glu242Asp
  variant of: http://identifiers.org/hgnc/23244
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119707
  ensembl protein: ENSP00000434444
  ensembl transcript: ENST00000528081
  gene symbol: RBM25
  hgvsc: ENST00000528081.1:c.*278G>C
  variant of: http://identifiers.org/hgnc/23244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16642
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu242Asp
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 2475
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8385
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555306706482518e-5
allele num: 64296
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e0

DP
type: SiteQuality
SIO_000300: 1.552832e6

VQSLOD
type: SiteQuality
SIO_000300: -6.959e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

BaseQRankSum
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SIO_000300: 1.28e0

InbreedingCoeff
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SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.0494e1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.922e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8320
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9856
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

South Asian
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allele frequency: 6.513809275664408e-5
allele num: 15352
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.517e1

FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 1.1e-3

MQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 7.54e-1

ReadPosRankSum
type: SiteQuality
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MQ
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

DP
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.275e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.742787200559538e-5
allele num: 11438
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.071913494915983e-5
allele num: 65106
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 15482
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.38e-1

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

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.507e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.282e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10044
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15604
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

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

European (Non-Finnish)
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allele count: 1
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allele num: 65312
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 890
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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.27e0

FS
type: SiteQuality
SIO_000300: 6.882e0

QD
type: SiteQuality
SIO_000300: 1.717e1

MQRankSum
type: SiteQuality
SIO_000300: -1.442e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.688683e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.527090587013621e-5
allele num: 65484
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

Latino
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allele count: 0
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Other
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African
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allele count: 0
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South Asian
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.86e-1

GenotypeQuality
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variant carriers: 0

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

East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 6.125199068969742e-5
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African
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Latino
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Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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BaseQRankSum
type: SiteQuality
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VQSLOD
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QD
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ReadPosRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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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variant carriers: 0

European (Finnish)
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num of homozygotes: 0

South Asian
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Latino
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East Asian
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African
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European (Non-Finnish)
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Other
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -9.206e-1

ClippingRankSum
type: SiteQuality
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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QD
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BaseQRankSum
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DP
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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Other
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African
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South Asian
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
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BaseQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4818
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -6.507e0

DP
type: SiteQuality
SIO_000300: 1.749292e6

VQSLOD
type: SiteQuality
SIO_000300: -1.85e0

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-1

FS
type: SiteQuality
SIO_000300: 1.4286e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.138e1

GenotypeQuality
all individuals: 3839
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99805126667666e-5
allele num: 66710
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e0

MQRankSum
type: SiteQuality
SIO_000300: -2.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.447e1

VQSLOD
type: SiteQuality
SIO_000300: 7.07e-1

FS
type: SiteQuality
SIO_000300: 7.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.49e-1

DP
type: SiteQuality
SIO_000300: 1.749418e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.693e0

VQSLOD
type: SiteQuality
SIO_000300: -7.6e-2

DP
type: SiteQuality
SIO_000300: 1.749682e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.535e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.421e0

QD
type: SiteQuality
SIO_000300: 1.581e1

MQRankSum
type: SiteQuality
SIO_000300: -1.283e0

GenotypeQuality
all individuals: 3265
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 32

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 25
allele frequency: 2.403846153846154e-3
allele num: 10400
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.994844433786943e-5
allele num: 66724
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: 16508
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.528e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
SIO_000300: 5.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.752195e6

MQRankSum
type: SiteQuality
SIO_000300: 2.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

GenotypeQuality
all individuals: 27952
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 8692
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variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.56e-1

DP
type: SiteQuality
SIO_000300: 1.751848e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 2.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-2

QD
type: SiteQuality
SIO_000300: 1.234e1

VQSLOD
type: SiteQuality
SIO_000300: 7.09e-1

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 27955
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.56e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.205e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.85e-1

GenotypeQuality
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variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.29e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.578e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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BaseQRankSum
type: SiteQuality
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QD
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FS
type: SiteQuality
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VQSLOD
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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
all individuals: 8108
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

FS
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27945
bin: 6.25e1
variant carriers: 0

African
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allele count: 3
allele frequency: 2.882952142994427e-4
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.87e1

FS
type: SiteQuality
SIO_000300: 4.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

DP
type: SiteQuality
SIO_000300: 1.753608e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.108e0

VQSLOD
type: SiteQuality
SIO_000300: 7.14e-1

MQRankSum
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QD
type: SiteQuality
SIO_000300: 1.301e1

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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variant carriers: 0

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

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

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
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South Asian
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MQRankSum
type: SiteQuality
SIO_000300: -2.95e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
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SIO_000300: 1.753703e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

VQSLOD
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InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.54e-1

QD
type: SiteQuality
SIO_000300: 1.003e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.77e-1

GenotypeQuality
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variant carriers: 0

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

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

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

African
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allele count: 5
allele frequency: 4.804920238324044e-4
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 2.444e0

QD
type: SiteQuality
SIO_000300: 1.231e1

InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.35e0

MQRankSum
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SIO_000300: -1.71e-1

DP
type: SiteQuality
SIO_000300: 1.754117e6

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.936e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-1

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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variant carriers: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.04890913450012e-4
allele num: 66736
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 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 count: 0
allele frequency: 0.0e0
allele num: 11578
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
allele num: 16512
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.75e-1

DP
type: SiteQuality
SIO_000300: 1.754333e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.284e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 7.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.826e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

ClippingRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e0

VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.753986e6

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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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
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 frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 0.0e0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

African
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allele frequency: 9.609840476648087e-5
allele num: 10406
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South Asian
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Other
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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

European (Finnish)
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East Asian
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MQ
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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FS
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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allele num: 66714
num of homozygotes: 0

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

European (Non-Finnish)
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num of homozygotes: 0

African
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East Asian
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South Asian
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Latino
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allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.359e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.94e-1

DP
type: SiteQuality
SIO_000300: 1.753251e6

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

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4834
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.739e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

DP
type: SiteQuality
SIO_000300: 1.753012e6

QD
type: SiteQuality
SIO_000300: 8.369999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -2.757e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.87e-1

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8723
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.46e-1

QD
type: SiteQuality
SIO_000300: 1.178e1

VQSLOD
type: SiteQuality
SIO_000300: -3.321e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.436e0

FS
type: SiteQuality
SIO_000300: 7.104e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

DP
type: SiteQuality
SIO_000300: 1.752163e6

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1683
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variant carriers: 0

GenotypeQuality
all individuals: 8055
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

VQSLOD
type: SiteQuality
SIO_000300: 4.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e0

QD
type: SiteQuality
SIO_000300: 1.248e1

DP
type: SiteQuality
SIO_000300: 1.749734e6

MQRankSum
type: SiteQuality
SIO_000300: -6.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.068e0

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 3.75e1
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GenotypeQuality
all individuals: 8723
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27196
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1683
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.749227e6

MQRankSum
type: SiteQuality
SIO_000300: -4.92e-1

QD
type: SiteQuality
SIO_000300: 1.059e1

GenotypeQuality
all individuals: 8724
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3264
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2307
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4824
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

FS
type: SiteQuality
SIO_000300: 4.299e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.09e-1

DP
type: SiteQuality
SIO_000300: 1.74956e6

QD
type: SiteQuality
SIO_000300: 1.371e1

VQSLOD
type: SiteQuality
SIO_000300: 9.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-2

MQ
type: SiteQuality
SIO_000300: 5.955e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

GenotypeQuality
all individuals: 27043
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4820
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1680
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8774
bin: 9.75e1
variant carriers: 81

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2303
bin: 9.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.454828122300915e-4
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 75
allele frequency: 7.210151893866564e-3
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.331e1

FS
type: SiteQuality
SIO_000300: 1.339e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.028e0

MQRankSum
type: SiteQuality
SIO_000300: -1.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.73e0

DP
type: SiteQuality
SIO_000300: 1.75516e6

GenotypeQuality
all individuals: 195
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3836
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4819
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variant carriers: 0

GenotypeQuality
all individuals: 8756
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 261
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2305
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26940
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 3.666e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

QD
type: SiteQuality
SIO_000300: 1.33e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.23e0

DP
type: SiteQuality
SIO_000300: 1.750875e6

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1382
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 226
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 87
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22157
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 17714
bin: 9.75e1
variant carriers: 10463

GenotypeQuality
all individuals: 3112
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 6623
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2665
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1888
bin: 9.25e1
variant carriers: 8

African
type: Population
allele count: 551
allele frequency: 5.297058258027303e-2
allele num: 10402
num of homozygotes: 11

East Asian
type: Population
allele count: 1721
allele frequency: 1.992820750347383e-1
allele num: 8636
num of homozygotes: 183

Other
type: Population
allele count: 103
allele frequency: 1.139380530973451e-1
allele num: 904
num of homozygotes: 11

Latino
type: Population
allele count: 667
allele frequency: 5.761921216309606e-2
allele num: 11576
num of homozygotes: 21

South Asian
type: Population
allele count: 986
allele frequency: 5.999026527135556e-2
allele num: 16436
num of homozygotes: 38

European (Finnish)
type: Population
allele count: 440
allele frequency: 6.652555185969157e-2
allele num: 6614
num of homozygotes: 18

European (Non-Finnish)
type: Population
allele count: 6659
allele frequency: 9.988899555982239e-2
allele num: 66664
num of homozygotes: 342

VQSLOD
type: SiteQuality
SIO_000300: 4.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-1

QD
type: SiteQuality
SIO_000300: 1.593e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 6.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.55e-2

DP
type: SiteQuality
SIO_000300: 2.373218e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

GenotypeQuality
all individuals: 4289
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1635
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22622
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7036
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3551
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2398
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.58e-1

QD
type: SiteQuality
SIO_000300: 1.452e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.15e0

FS
type: SiteQuality
SIO_000300: 1.149e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

DP
type: SiteQuality
SIO_000300: 2.045064e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.628e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
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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allele count: 2
allele frequency: 2.313208420078649e-4
allele num: 8646
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

FS
type: SiteQuality
SIO_000300: 2.929e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.75e-1

ClippingRankSum
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SIO_000300: -1.285e0

QD
type: SiteQuality
SIO_000300: 1.713e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.6e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Latino
type: Population
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
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.004743747560573e-5
allele num: 66614
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.037933e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.28e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.778e0

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.343e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

FS
type: SiteQuality
SIO_000300: 1.779e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 3.456022118541559e-4
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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

QD
type: SiteQuality
SIO_000300: 1.387e1

FS
type: SiteQuality
SIO_000300: 4.436e0

VQSLOD
type: SiteQuality
SIO_000300: 7.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.171e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e-1

DP
type: SiteQuality
SIO_000300: 2.037565e6

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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bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 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: 16332
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.88e0

VQSLOD
type: SiteQuality
SIO_000300: -4.49e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.74e-1

FS
type: SiteQuality
SIO_000300: 1.645e0

QD
type: SiteQuality
SIO_000300: 3.479e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

DP
type: SiteQuality
SIO_000300: 2.036579e6

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1816
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10136
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1200
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.51e-1

DP
type: SiteQuality
SIO_000300: 5.06612e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.419999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.701e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 938
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.904036557501904e-4
allele num: 5252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 360
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7894
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.31e0

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.99648e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.96e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

MQ
type: SiteQuality
SIO_000300: 5.799e1

QD
type: SiteQuality
SIO_000300: 1.376e1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

Latino
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allele count: 3
allele frequency: 9.933774834437087e-3
allele num: 302
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
type: Population
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allele frequency: 1.288327750579748e-4
allele num: 7762
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 59
allele frequency: 7.125603864734299e-2
allele num: 828
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.216312056737589e-4
allele num: 4512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.779999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
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QD
type: SiteQuality
SIO_000300: 1.449e1

VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 304
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African
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East Asian
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Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 1.288327750579748e-4
allele num: 7762
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.91e1

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.74e-1

QD
type: SiteQuality
SIO_000300: 1.002e1

DP
type: SiteQuality
SIO_000300: 3.60785e5

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.260000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4248
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Other
type: Population
allele count: 0
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African
type: Population
allele count: 0
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allele num: 720
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 1.297016861219196e-4
allele num: 7710
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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

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.25e-2

ClippingRankSum
type: SiteQuality
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MQRankSum
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SIO_000300: -2.87e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.693e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.57e0

DP
type: SiteQuality
SIO_000300: 3.4159e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.248e1

FS
type: SiteQuality
SIO_000300: 3.576e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7702
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.27e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.159e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

DP
type: SiteQuality
SIO_000300: 3.36044e5

GenotypeQuality
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bin: 7.5e0
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 24

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 3.13889615485221e-3
allele num: 7646
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3826
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.43e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.15084e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.38e-2

QD
type: SiteQuality
SIO_000300: 1.082e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.465e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-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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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 8
allele frequency: 8.125126955108674e-4
allele num: 9846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.934953538241601e-5
allele num: 11192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8188
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

FS
type: SiteQuality
SIO_000300: 3.031e0

DP
type: SiteQuality
SIO_000300: 1.585358e6

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

QD
type: SiteQuality
SIO_000300: 1.354e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.339e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1017
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11262
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64876
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.011326860841424e-4
allele num: 9888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 8.25e0

FS
type: SiteQuality
SIO_000300: 7.128e0

VQSLOD
type: SiteQuality
SIO_000300: 3.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.27e-1

QD
type: SiteQuality
SIO_000300: 1.612e1

MQ
type: SiteQuality
SIO_000300: 5.902e1

DP
type: SiteQuality
SIO_000300: 1.620326e6

MQRankSum
type: SiteQuality
SIO_000300: 8.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

GenotypeQuality
all individuals: 7216
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
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variant carriers: 0

GenotypeQuality
all individuals: 22
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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
all individuals: 2126
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GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9978
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.19047619047619e-4
allele num: 8400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.82e0

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.67e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 1.706919e6

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 7245
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.188777936281503e-4
allele num: 8412
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.001602564102564e-4
allele num: 9984
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65800
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.710357e6

FS
type: SiteQuality
SIO_000300: 7.269e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQRankSum
type: SiteQuality
SIO_000300: 8.88e-1

QD
type: SiteQuality
SIO_000300: 1.374e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.01e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.088650754992694e-5
allele num: 16424
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10000
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Other
type: Population
allele count: 0
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allele num: 898
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.133e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e-1

DP
type: SiteQuality
SIO_000300: 1.716325e6

MQRankSum
type: SiteQuality
SIO_000300: -1.16e0

QD
type: SiteQuality
SIO_000300: 1.301e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.706e0

VQSLOD
type: SiteQuality
SIO_000300: 4.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.78e-1

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510163399679845e-5
allele num: 66218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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East Asian
type: Population
allele count: 1
allele frequency: 1.173708920187793e-4
allele num: 8520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.533e1

FS
type: SiteQuality
SIO_000300: 7.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.63e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.78e0

MQRankSum
type: SiteQuality
SIO_000300: 7.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.72509e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2157
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GenotypeQuality
all individuals: 180
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10048
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510163399679845e-5
allele num: 66218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.63e-1

QD
type: SiteQuality
SIO_000300: 1.533e1

VQSLOD
type: SiteQuality
SIO_000300: 3.91e0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.72509e6

MQ
type: SiteQuality
SIO_000300: 5.937e1

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5725
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36229
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7436
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2775
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3418
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 2.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.736e0

QD
type: SiteQuality
SIO_000300: 1.035e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

VQSLOD
type: SiteQuality
SIO_000300: -1.259e0

DP
type: SiteQuality
SIO_000300: 1.734256e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 3409
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2768
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2150
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 296
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7421
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5778
bin: 9.75e1
variant carriers: 84

GenotypeQuality
all individuals: 898
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 8.865248226950354e-4
allele num: 10152
num of homozygotes: 1

Latino
type: Population
allele count: 2
allele frequency: 1.73460537727667e-4
allele num: 11530
num of homozygotes: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 73
allele frequency: 1.097315335357604e-3
allele num: 66526
num of homozygotes: 1

DP
type: SiteQuality
SIO_000300: 1.738438e6

VQSLOD
type: SiteQuality
SIO_000300: 4.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.868e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

QD
type: SiteQuality
SIO_000300: 1.297e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.08e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

FS
type: SiteQuality
SIO_000300: 7.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.72e-1

GenotypeQuality
all individuals: 166
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36653
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7475
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 5702
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3417
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
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: 16500
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-1

QD
type: SiteQuality
SIO_000300: 1.593e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.738985e6

FS
type: SiteQuality
SIO_000300: 4.575e0

VQSLOD
type: SiteQuality
SIO_000300: 2.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.43e0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36800
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3418
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7510
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

DP
type: SiteQuality
SIO_000300: 1.741837e6

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

QD
type: SiteQuality
SIO_000300: 1.044e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 5702
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2157
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2785
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7511
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36818
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3416
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.977e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 4.995e0

DP
type: SiteQuality
SIO_000300: 1.742163e6

MQRankSum
type: SiteQuality
SIO_000300: -2.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.87e-1

QD
type: SiteQuality
SIO_000300: 1.197e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.292e0

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

GenotypeQuality
all individuals: 36797
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7495
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1247
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2782
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5776
bin: 9.75e1
variant carriers: 74

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

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

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

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

Latino
type: Population
allele count: 73
allele frequency: 6.310511756569848e-3
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.659969088098918e-5
allele num: 10352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.25e-1

FS
type: SiteQuality
SIO_000300: 5.55e-1

DP
type: SiteQuality
SIO_000300: 1.746696e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

QD
type: SiteQuality
SIO_000300: 1.365e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

GenotypeQuality
all individuals: 2782
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3410
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 899
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2155
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36797
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 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: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.746696e6

QD
type: SiteQuality
SIO_000300: 1.365e1

MQ
type: SiteQuality
SIO_000300: 5.943e1

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

FS
type: SiteQuality
SIO_000300: 5.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 899
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7511
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2786
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2161
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5707
bin: 9.75e1
variant carriers: 2

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

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.919e1

DP
type: SiteQuality
SIO_000300: 1.743302e6

QD
type: SiteQuality
SIO_000300: 1.397e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.3e-1

FS
type: SiteQuality
SIO_000300: 4.976e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36834
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2787
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5709
bin: 9.75e1
variant carriers: 3

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

African
type: Population
allele count: 2
allele frequency: 1.928268414963363e-4
allele num: 10372
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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MQRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQ
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 1.498800959232614e-5
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Latino
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Other
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East Asian
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FS
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QD
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VQSLOD
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ClippingRankSum
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DP
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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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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African
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Other
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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BaseQRankSum
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VQSLOD
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MQRankSum
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FS
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MQ
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QD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66718
num of homozygotes: 0

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