14-23374359-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374359
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374359
    reference: chr 14
allele count: 3
allele frequency: 2.484595507851322e-5
allele num: 120744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.160A>G
  hgvsp: ENSP00000438504.2:p.Ile54Val
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.328A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.670A>G
  hgvsp: ENSP00000352956.3:p.Ile224Val
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.563A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.818A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.622A>G
  hgvsp: ENSP00000382806.2:p.Ile208Val
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.831A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-81A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.160A>G
  hgvsp: ENSP00000452171.1:p.Ile54Val
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.568A>G
  hgvsp: ENSP00000339220.5:p.Ile190Val
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6612
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile224Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

14-23374369-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374369
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374369
    reference: chr 14
allele count: 1
allele frequency: 8.281710670156027e-6
allele num: 120748
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.660G>A
  hgvsp: ENST00000359890.3:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.553G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.150G>A
  hgvsp: ENST00000555722.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.150G>A
  hgvsp: ENST00000557403.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-91G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.558G>A
  hgvsp: ENST00000346528.5:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.808G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.612G>A
  hgvsp: ENST00000399922.2:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.150G>A
  hgvsp: ENST00000542016.2:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.821G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.318G>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val220Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/14-23374375-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374375
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374375
    reference: chr 14
allele count: 2
allele frequency: 1.656314699792961e-5
allele num: 120750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.144G>T
  hgvsp: ENSP00000438504.2:p.Gln48His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-97G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.606G>T
  hgvsp: ENSP00000382806.2:p.Gln202His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.552G>T
  hgvsp: ENSP00000339220.5:p.Gln184His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.654G>T
  hgvsp: ENSP00000352956.3:p.Gln218His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.144G>T
  hgvsp: ENSP00000450556.1:p.Gln48His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.802G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.144G>T
  hgvsp: ENSP00000452171.1:p.Gln48His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.547G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.815G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.312G>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln218His
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

14-23374377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374377
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374377
    reference: chr 14
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.550C>T
  hgvsp: ENSP00000339220.5:p.Gln184Ter
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.652C>T
  hgvsp: ENSP00000352956.3:p.Gln218Ter
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.142C>T
  hgvsp: ENSP00000438504.2:p.Gln48Ter
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.604C>T
  hgvsp: ENSP00000382806.2:p.Gln202Ter
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.142C>T
  hgvsp: ENSP00000450556.1:p.Gln48Ter
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.310C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.142C>T
  hgvsp: ENSP00000452171.1:p.Gln48Ter
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.545C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.800C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-99C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.813C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln218Ter
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

14-23374396-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374396
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374396
    reference: chr 14
allele count: 2
allele frequency: 1.656369569178275e-5
allele num: 120746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.123C>T
  hgvsp: ENST00000555722.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.123C>T
  hgvsp: ENST00000542016.2:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.633C>T
  hgvsp: ENST00000359890.3:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.585C>T
  hgvsp: ENST00000399922.2:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.123C>T
  hgvsp: ENST00000557403.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.291C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.526C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.781C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.531C>T
  hgvsp: ENST00000346528.5:c.531C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-118C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.794C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr211Tyr
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

14-23374401-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374401
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374401
    reference: chr 14
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.628G>A
  hgvsp: ENSP00000352956.3:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-123G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.118G>A
  hgvsp: ENSP00000452171.1:p.Ala40Thr
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.118G>A
  hgvsp: ENSP00000450556.1:p.Ala40Thr
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.526G>A
  hgvsp: ENSP00000339220.5:p.Ala176Thr
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.580G>A
  hgvsp: ENSP00000382806.2:p.Ala194Thr
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.521G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.789G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.286G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.118G>A
  hgvsp: ENSP00000438504.2:p.Ala40Thr
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.776G>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6369
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala210Thr
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

14-23374402-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374402
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374402
    reference: chr 14
allele count: 2
allele frequency: 1.656342134031205e-5
allele num: 120748
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.775T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.285T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.579T>C
  hgvsp: ENST00000399922.2:c.579T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.627T>C
  hgvsp: ENST00000359890.3:c.627T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.520T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.788T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.525T>C
  hgvsp: ENST00000346528.5:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.117T>C
  hgvsp: ENST00000542016.2:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.117T>C
  hgvsp: ENST00000557403.1:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.117T>C
  hgvsp: ENST00000555722.1:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-124T>C
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile209Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum

14-23374419-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374419
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374419
    reference: chr 14
allele count: 2
allele frequency: 1.656589083077942e-5
allele num: 120730
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.610C>T
  hgvsp: ENSP00000352956.3:p.Arg204Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-141C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.100C>T
  hgvsp: ENSP00000450556.1:p.Arg34Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.771C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.503C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.508C>T
  hgvsp: ENSP00000339220.5:p.Arg170Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.100C>T
  hgvsp: ENSP00000452171.1:p.Arg34Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.562C>T
  hgvsp: ENSP00000382806.2:p.Arg188Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.100C>T
  hgvsp: ENSP00000438504.2:p.Arg34Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.758C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.268C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg204Cys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

14-23374420-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374420
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374420
    reference: chr 14
allele count: 2
allele frequency: 1.656561640658649e-5
allele num: 120732
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.267A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.561A>G
  hgvsp: ENST00000399922.2:c.561A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.99A>G
  hgvsp: ENST00000557403.1:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.770A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-142A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.99A>G
  hgvsp: ENST00000555722.1:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.507A>G
  hgvsp: ENST00000346528.5:c.507A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.609A>G
  hgvsp: ENST00000359890.3:c.609A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.757A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.99A>G
  hgvsp: ENST00000542016.2:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.502A>G
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser203Ser
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

14-23374427-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374427
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374427
    reference: chr 14
allele count: 1
allele frequency: 8.282945415389712e-6
allele num: 120730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.92G>A
  hgvsp: ENSP00000450556.1:p.Arg31Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.554G>A
  hgvsp: ENSP00000382806.2:p.Arg185Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.495G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.92G>A
  hgvsp: ENSP00000452171.1:p.Arg31Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.500G>A
  hgvsp: ENSP00000339220.5:p.Arg167Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-149G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.602G>A
  hgvsp: ENSP00000352956.3:p.Arg201Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.750G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.763G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.260G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.92G>A
  hgvsp: ENSP00000438504.2:p.Arg31Gln
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg201Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

14-23374428-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374428
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374428
    reference: chr 14
allele count: 4
allele frequency: 3.313287941288538e-5
allele num: 120726
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.749C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.91C>T
  hgvsp: ENSP00000438504.2:p.Arg31Trp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.259C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.499C>T
  hgvsp: ENSP00000339220.5:p.Arg167Trp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.91C>T
  hgvsp: ENSP00000452171.1:p.Arg31Trp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.762C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.91C>T
  hgvsp: ENSP00000450556.1:p.Arg31Trp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.601C>T
  hgvsp: ENSP00000352956.3:p.Arg201Trp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-150C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.553C>T
  hgvsp: ENSP00000382806.2:p.Arg185Trp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.494C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg201Trp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

14-23374432-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374432
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374432
    reference: chr 14
allele count: 1
allele frequency: 8.283082632032337e-6
allele num: 120728
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-2A>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.758A>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.745A>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.87A>C
  hgvsp: ENST00000542016.2:c.87A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.549A>C
  hgvsp: ENST00000399922.2:c.549A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.87A>C
  hgvsp: ENST00000555722.1:c.87A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.495A>C
  hgvsp: ENST00000346528.5:c.495A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.490A>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.597A>C
  hgvsp: ENST00000359890.3:c.597A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.87A>C
  hgvsp: ENST00000557403.1:c.87A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.255A>C
  variant of: http://identifiers.org/hgnc/20155
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-152-2A>C
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

14-23374435-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374435
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374435
    reference: chr 14
allele count: 70018
allele frequency: 5.802724922097726e-1
allele num: 120664
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.492C>T
  hgvsp: ENST00000346528.5:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.594C>T
  hgvsp: ENST00000359890.3:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.252C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.546C>T
  hgvsp: ENST00000399922.2:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.84C>T
  hgvsp: ENST00000542016.2:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.487C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.755C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.84C>T
  hgvsp: ENST00000555722.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.742C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-5C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.84C>T
  hgvsp: ENST00000557403.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 6.25e1
  variant carriers: 4517
genotype depth: GenotypeDepth
  all individuals: 8165
  bin: 9.75e1
  variant carriers: 7583
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 6.75e1
  variant carriers: 4499
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 8.25e1
  variant carriers: 3304
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 2.25e1
  variant carriers: 236
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4297
  bin: 7.75e1
  variant carriers: 3796
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 2.75e1
  variant carriers: 503
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 3.25e1
  variant carriers: 859
genotype depth: GenotypeDepth
  all individuals: 5331
  bin: 5.75e1
  variant carriers: 4140
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 3.75e1
  variant carriers: 1370
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 4.25e1
  variant carriers: 2101
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 7.25e1
  variant carriers: 4358
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 9.25e1
  variant carriers: 2086
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 4.75e1
  variant carriers: 2823
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 5.25e1
  variant carriers: 3516
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 8.75e1
  variant carriers: 2433
genotype quality: GenotypeQuality
hgvs: c.-152-5C>T
num of homozygotes: 21771
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

14-23374437-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374437
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374437
    reference: chr 14
allele count: 1
allele frequency: 8.28775070445881e-6
allele num: 120660
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.490A>G
  hgvsp: ENSP00000339220.5:p.Ile164Val
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.82A>G
  hgvsp: ENSP00000452171.1:p.Ile28Val
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.544A>G
  hgvsp: ENSP00000382806.2:p.Ile182Val
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.82A>G
  hgvsp: ENSP00000450556.1:p.Ile28Val
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.740A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.82A>G
  hgvsp: ENSP00000438504.2:p.Ile28Val
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.592A>G
  hgvsp: ENSP00000352956.3:p.Ile198Val
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-7A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.753A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.250A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.485A>G
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5766
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4420
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile198Val
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/14-23374442-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374442
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374442
    reference: chr 14
allele count: 1
allele frequency: 8.289811821271656e-6
allele num: 120630
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.748G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.539G>T
  hgvsp: ENSP00000382806.2:p.Arg180Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.77G>T
  hgvsp: ENSP00000452171.1:p.Arg26Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.77G>T
  hgvsp: ENSP00000438504.2:p.Arg26Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-12G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.587G>T
  hgvsp: ENSP00000352956.3:p.Arg196Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.245G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.77G>T
  hgvsp: ENSP00000450556.1:p.Arg26Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.735G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.480G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.485G>T
  hgvsp: ENSP00000339220.5:p.Arg162Leu
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg196Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

14-23374442-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374442
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374442
    reference: chr 14
allele count: 9
allele frequency: 7.460830639144492e-5
allele num: 120630
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.77G>A
  hgvsp: ENSP00000450556.1:p.Arg26His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.77G>A
  hgvsp: ENSP00000452171.1:p.Arg26His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.485G>A
  hgvsp: ENSP00000339220.5:p.Arg162His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.587G>A
  hgvsp: ENSP00000352956.3:p.Arg196His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-12G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.735G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.539G>A
  hgvsp: ENSP00000382806.2:p.Arg180His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.245G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.748G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.77G>A
  hgvsp: ENSP00000438504.2:p.Arg26His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.480G>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5604
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg196His
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

14-23374443-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374443
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374443
    reference: chr 14
allele count: 6
allele frequency: 4.973804628954175e-5
allele num: 120632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.747C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.76C>T
  hgvsp: ENSP00000452171.1:p.Arg26Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.586C>T
  hgvsp: ENSP00000352956.3:p.Arg196Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.734C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.479C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.484C>T
  hgvsp: ENSP00000339220.5:p.Arg162Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.76C>T
  hgvsp: ENSP00000438504.2:p.Arg26Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.538C>T
  hgvsp: ENSP00000382806.2:p.Arg180Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.244C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.76C>T
  hgvsp: ENSP00000450556.1:p.Arg26Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-13C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5766
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg196Cys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

14-23374449-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374449
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374449
    reference: chr 14
allele count: 1
allele frequency: 8.292561572269675e-6
allele num: 120590
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.238G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.473G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.70G>C
  hgvsp: ENSP00000438504.2:p.Asp24His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.70G>C
  hgvsp: ENSP00000450556.1:p.Asp24His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.478G>C
  hgvsp: ENSP00000339220.5:p.Asp160His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.532G>C
  hgvsp: ENSP00000382806.2:p.Asp178His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.580G>C
  hgvsp: ENSP00000352956.3:p.Asp194His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.741G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-19G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.70G>C
  hgvsp: ENSP00000452171.1:p.Asp24His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.728G>C
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp194His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

14-23374449-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374449
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374449
    reference: chr 14
allele count: 10
allele frequency: 8.292561572269674e-5
allele num: 120590
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.532G>A
  hgvsp: ENSP00000382806.2:p.Asp178Asn
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.478G>A
  hgvsp: ENSP00000339220.5:p.Asp160Asn
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.728G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.741G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.70G>A
  hgvsp: ENSP00000452171.1:p.Asp24Asn
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.580G>A
  hgvsp: ENSP00000352956.3:p.Asp194Asn
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.70G>A
  hgvsp: ENSP00000438504.2:p.Asp24Asn
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-19G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.473G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.70G>A
  hgvsp: ENSP00000450556.1:p.Asp24Asn
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.238G>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp194Asn
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

14-23374450-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374450
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374450
    reference: chr 14
allele count: 5
allele frequency: 4.146005738071942e-5
allele num: 120598
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.579C>T
  hgvsp: ENST00000359890.3:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.472C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.740C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.69C>T
  hgvsp: ENST00000555722.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.69C>T
  hgvsp: ENST00000557403.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.69C>T
  hgvsp: ENST00000542016.2:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.237C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.531C>T
  hgvsp: ENST00000399922.2:c.531C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.727C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-20C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.477C>T
  hgvsp: ENST00000346528.5:c.477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5598
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg193Arg
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

14-23374451-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374451
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374451
    reference: chr 14
allele count: 17
allele frequency: 1.409758848309948e-4
allele num: 120588
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.68G>A
  hgvsp: ENSP00000450556.1:p.Arg23His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.471G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.476G>A
  hgvsp: ENSP00000339220.5:p.Arg159His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.739G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.726G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.578G>A
  hgvsp: ENSP00000352956.3:p.Arg193His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.68G>A
  hgvsp: ENSP00000452171.1:p.Arg23His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.68G>A
  hgvsp: ENSP00000438504.2:p.Arg23His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-21G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.530G>A
  hgvsp: ENSP00000382806.2:p.Arg177His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.236G>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg193His
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

14-23374452-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374452
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374452
    reference: chr 14
allele count: 5
allele frequency: 4.146349553852788e-5
allele num: 120588
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.235C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.529C>T
  hgvsp: ENSP00000382806.2:p.Arg177Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.725C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.577C>T
  hgvsp: ENSP00000352956.3:p.Arg193Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.67C>T
  hgvsp: ENSP00000450556.1:p.Arg23Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.475C>T
  hgvsp: ENSP00000339220.5:p.Arg159Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.67C>T
  hgvsp: ENSP00000438504.2:p.Arg23Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.67C>T
  hgvsp: ENSP00000452171.1:p.Arg23Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-22C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.738C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.470C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg193Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

14-23374462-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374462
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374462
    reference: chr 14
allele count: 1
allele frequency: 8.298204268596276e-6
allele num: 120508
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.526-7T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.472-7T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.735-7T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.722-7T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.467-7T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.64-7T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.232-7T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.574-7T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.64-7T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-32T>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.64-7T>C
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.574-7T>C
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

14-23374463-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374463
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374463
    reference: chr 14
allele count: 1
allele frequency: 8.297928836962294e-6
allele num: 120512
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.574-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.472-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.232-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.722-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.735-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.526-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-33C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.467-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.64-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.64-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.64-8C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.574-8C>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: G
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-23374466-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374466
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374466
    reference: chr 14
allele count: 6
allele frequency: 4.979914345473258e-5
allele num: 120484
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.64-11G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.722-11G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-36G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.64-11G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.526-11G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.467-11G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.64-11G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.232-11G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.472-11G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.735-11G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.574-11G>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

14-23374467-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374467
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374467
    reference: chr 14
allele count: 5
allele frequency: 4.149859734740966e-5
allele num: 120486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.64-12C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.232-12C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.467-12C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.526-12C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-37C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.735-12C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.574-12C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.722-12C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.64-12C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.64-12C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.472-12C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

14-23374473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374473
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374473
    reference: chr 14
allele count: 3
allele frequency: 2.490618669677548e-5
allele num: 120452
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.574-18C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-43C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.722-18C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.735-18C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.232-18C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.467-18C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.472-18C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.64-18C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.64-18C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.64-18C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.526-18C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

14-23374475-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374475
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374475
    reference: chr 14
allele count: 1
allele frequency: 8.302200083022e-6
allele num: 120450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.232-20T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-45T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.526-20T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.467-20T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.722-20T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.472-20T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.574-20T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.64-20T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.735-20T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.64-20T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.64-20T>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3062
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-23374478-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374478
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374478
    reference: chr 14
allele count: 2
allele frequency: 1.660826094899603e-5
allele num: 120422
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.472-23G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.722-23G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.64-23G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.467-23G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-48G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.735-23G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.64-23G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.526-23G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.232-23G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.64-23G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.574-23G>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5766
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2712
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

14-23374480-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374480
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374480
    reference: chr 14
allele count: 1
allele frequency: 8.303854649328218e-6
allele num: 120426
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.232-25A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.574-25A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.64-25A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-152-50A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.64-25A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.722-25A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.526-25A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.467-25A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.735-25A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.472-25A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.64-25A>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-23374488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374488
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374488
    reference: chr 14
allele count: 1
allele frequency: 8.30827005200977e-6
allele num: 120362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.64-33C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.64-33C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.64-33C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.526-33C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-153+57C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.467-33C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.735-33C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.472-33C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.722-33C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.232-33C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.574-33C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

14-23374489-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374489
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374489
    reference: chr 14
allele count: 1
allele frequency: 8.30827005200977e-6
allele num: 120362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.467-34G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.64-34G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.64-34G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.735-34G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-153+56G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.574-34G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.472-34G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.722-34G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.526-34G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.64-34G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.232-34G>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

14-23374495-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374495
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374495
    reference: chr 14
allele count: 1
allele frequency: 8.30923654734603e-6
allele num: 120348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.472-40C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.64-40C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.526-40C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.735-40C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.64-40C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.64-40C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-153+50C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.722-40C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.467-40C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.232-40C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.574-40C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

14-23374501-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374501
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374501
    reference: chr 14
allele count: 4
allele frequency: 3.324412825584681e-5
allele num: 120322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.63+44A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.573+44A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.63+44A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.231+44A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.721+44A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.734+44A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-153+44A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.466+44A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.471+44A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.525+44A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.63+44A>G
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49522
  bin: 9.75e1
  variant carriers: 4
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

14-23374504-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374504
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374504
    reference: chr 14
allele count: 2
allele frequency: 1.662427476601333e-5
allele num: 120306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.63+41T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-153+41T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.525+41T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.231+41T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.63+41T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.573+41T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.63+41T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.466+41T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.721+41T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.471+41T>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.734+41T>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

14-23374513-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374513
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374513
    reference: chr 14
allele count: 3
allele frequency: 2.493931433511788e-5
allele num: 120292
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.63+32A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.231+32A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.63+32A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.721+32A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.573+32A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.525+32A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.63+32A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.471+32A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.466+32A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.734+32A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-153+32A>G
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1369
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD

14-23374519-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374519
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374519
    reference: chr 14
allele count: 3
allele frequency: 2.4942631946523e-5
allele num: 120276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.466+26C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.63+26C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.231+26C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-153+26C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.734+26C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.525+26C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.721+26C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.63+26C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.471+26C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.63+26C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.573+26C>G
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1237
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-23374524-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374524
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374524
    reference: chr 14
allele count: 10
allele frequency: 8.315040244794785e-5
allele num: 120264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.466+21T>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.471+21T>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.573+21T>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.734+21T>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.525+21T>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.63+21T>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.231+21T>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.721+21T>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.63+21T>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-153+21T>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.63+21T>G
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum

14-23374535-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374535
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374535
    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: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-153+10C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.63+10C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.63+10C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.466+10C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.231+10C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.471+10C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.721+10C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.573+10C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.63+10C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.734+10C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.525+10C>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS

14-23374540-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374540
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374540
    reference: chr 14
allele count: 2
allele frequency: 1.663561352142667e-5
allele num: 120224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.231+5C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.471+5C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-153+5C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.63+5C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.63+5C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.466+5C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.525+5C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.721+5C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.734+5C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.573+5C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.63+5C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.573+5C>T
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

14-23374540-GTTACCTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374540
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374533
    reference: chr 14
allele count: 2
allele frequency: 1.663561352142667e-5
allele num: 120224
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.571_573+4delAAGGTAA
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.61_63+4delAAGGTAA
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.464_466+4delAAGGTAA
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.61_63+4delAAGGTAA
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.732_734+4delAAGGTAA
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.719_721+4delAAGGTAA
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.61_63+4delAAGGTAA
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.469_471+4delAAGGTAA
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: 5_prime_UTR_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-155_-153+4delAAGGTAA
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.229_231+4delAAGGTAA
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.523_525+4delAAGGTAA
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: splice donor
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.571_573+4delAAGGTAA
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: GTTACCTT
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

14-23374541-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374541
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374541
    reference: chr 14
allele count: 1
allele frequency: 8.317391665973551e-6
allele num: 120230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.231+4A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-153+4A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.525+4A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.734+4A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.721+4A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.63+4A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.63+4A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.466+4A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.573+4A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.63+4A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.471+4A>G
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.573+4A>G
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

14-23374545-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374545
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374545
    reference: chr 14
allele count: 2
allele frequency: 1.663506005256679e-5
allele num: 120228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.466G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.63G>A
  hgvsp: ENST00000557227.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.721G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.63G>A
  hgvsp: ENST00000542016.2:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.63G>A
  hgvsp: ENST00000555722.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.231G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.525G>A
  hgvsp: ENST00000399922.2:c.525G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.573G>A
  hgvsp: ENST00000359890.3:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.734G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.471G>A
  hgvsp: ENST00000346528.5:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.63G>A
  hgvsp: ENST00000557403.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.554G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-153G>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.573G>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

14-23374548-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374548
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374548
    reference: chr 14
allele count: 117
allele frequency: 9.731348249189054e-4
allele num: 120230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.468C>T
  hgvsp: ENST00000346528.5:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.718C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.463C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.60C>T
  hgvsp: ENST00000557227.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.551C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.228C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.60C>T
  hgvsp: ENST00000542016.2:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.570C>T
  hgvsp: ENST00000359890.3:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.731C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.60C>T
  hgvsp: ENST00000555722.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.522C>T
  hgvsp: ENST00000399922.2:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.60C>T
  hgvsp: ENST00000557403.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-156C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5757
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 8.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.Gly190Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

14-23374548-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374548
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374548
    reference: chr 14
allele count: 2
allele frequency: 1.66347833319471e-5
allele num: 120230
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.570C>G
  hgvsp: ENST00000359890.3:c.570C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.718C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.731C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-156C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.468C>G
  hgvsp: ENST00000346528.5:c.468C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.228C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.551C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.60C>G
  hgvsp: ENST00000557227.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.60C>G
  hgvsp: ENST00000542016.2:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.60C>G
  hgvsp: ENST00000555722.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.522C>G
  hgvsp: ENST00000399922.2:c.522C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.60C>G
  hgvsp: ENST00000557403.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.463C>G
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5361
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5757
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly190Gly
num of homozygotes: 1
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

14-23374548-GCCTACAGCAGAGAAAAAGTCCTCCAGATCTCGAGGCCGAATTCGGGCAGCTAACTGCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374548
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374490
    reference: chr 14
allele count: 2
allele frequency: 1.66347833319471e-5
allele num: 120230
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsp: ENSP00000452171.1:p.Met1_?20
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsp: ENSP00000352956.3:p.Met171ThrfsTer37
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsp: ENSP00000382806.2:p.Met155ThrfsTer37
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsp: ENSP00000438504.2:p.Met1_?20
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsp: ENSP00000450556.1:p.Met1_?20
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsp: ENSP00000450423.1:p.Met1_?20
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000555714
  gene symbol: RBM23
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsp: ENSP00000339220.5:p.Met137ThrfsTer37
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5361
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met171ThrfsTer37
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: GCCTACAGCAGAGAAAAAGTCCTCCAGATCTCGAGGCCGAATTCGGGCAGCTAACTGCA
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ

14-23374566-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374566
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374566
    reference: chr 14
allele count: 3
allele frequency: 2.495092983798529e-5
allele num: 120236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.42C>G
  hgvsp: ENSP00000450423.1:p.Asp14Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.450C>G
  hgvsp: ENSP00000339220.5:p.Asp150Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.504C>G
  hgvsp: ENSP00000382806.2:p.Asp168Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.42C>G
  hgvsp: ENSP00000438504.2:p.Asp14Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.42C>G
  hgvsp: ENSP00000452171.1:p.Asp14Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.700C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.42C>G
  hgvsp: ENSP00000450556.1:p.Asp14Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.552C>G
  hgvsp: ENSP00000352956.3:p.Asp184Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.445C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-174C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.533C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.210C>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.713C>G
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp184Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

14-23374566-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374566
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374566
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 120236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.504C>A
  hgvsp: ENSP00000382806.2:p.Asp168Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.533C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.552C>A
  hgvsp: ENSP00000352956.3:p.Asp184Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.450C>A
  hgvsp: ENSP00000339220.5:p.Asp150Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.445C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.210C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.42C>A
  hgvsp: ENSP00000450556.1:p.Asp14Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.42C>A
  hgvsp: ENSP00000438504.2:p.Asp14Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.42C>A
  hgvsp: ENSP00000450423.1:p.Asp14Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.42C>A
  hgvsp: ENSP00000452171.1:p.Asp14Glu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.713C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-174C>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.700C>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp184Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum

14-23374568-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374568
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374568
    reference: chr 14
allele count: 312
allele frequency: 2.594767219440795e-3
allele num: 120242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.40G>A
  hgvsp: ENSP00000450556.1:p.Asp14Asn
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.40G>A
  hgvsp: ENSP00000450423.1:p.Asp14Asn
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.40G>A
  hgvsp: ENSP00000438504.2:p.Asp14Asn
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.443G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-176G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.40G>A
  hgvsp: ENSP00000452171.1:p.Asp14Asn
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.550G>A
  hgvsp: ENSP00000352956.3:p.Asp184Asn
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.698G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.208G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.531G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.502G>A
  hgvsp: ENSP00000382806.2:p.Asp168Asn
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.711G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.448G>A
  hgvsp: ENSP00000339220.5:p.Asp150Asn
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 9.75e1
  variant carriers: 164
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 9.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 8.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
hgvs: p.Asp184Asn
num of homozygotes: 7
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

14-23374579-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374579
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374579
    reference: chr 14
allele count: 5
allele frequency: 4.158073315148693e-5
allele num: 120248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-187G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.29G>A
  hgvsp: ENSP00000450556.1:p.Arg10Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.539G>A
  hgvsp: ENSP00000352956.3:p.Arg180Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.520G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.432G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.437G>A
  hgvsp: ENSP00000339220.5:p.Arg146Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.491G>A
  hgvsp: ENSP00000382806.2:p.Arg164Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.29G>A
  hgvsp: ENSP00000450423.1:p.Arg10Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.700G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.29G>A
  hgvsp: ENSP00000438504.2:p.Arg10Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.29G>A
  hgvsp: ENSP00000452171.1:p.Arg10Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.197G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.687G>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5758
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg180Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

14-23374580-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374580
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374580
    reference: chr 14
allele count: 2
allele frequency: 1.66306336271412e-5
allele num: 120260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.196C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.28C>T
  hgvsp: ENSP00000450556.1:p.Arg10Ter
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.28C>T
  hgvsp: ENSP00000452171.1:p.Arg10Ter
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.28C>T
  hgvsp: ENSP00000438504.2:p.Arg10Ter
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.490C>T
  hgvsp: ENSP00000382806.2:p.Arg164Ter
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.686C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.436C>T
  hgvsp: ENSP00000339220.5:p.Arg146Ter
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.538C>T
  hgvsp: ENSP00000352956.3:p.Arg180Ter
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-188C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.699C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.28C>T
  hgvsp: ENSP00000450423.1:p.Arg10Ter
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.431C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.519C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5758
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg180Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

14-23374585-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374585
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374585
    reference: chr 14
allele count: 3
allele frequency: 2.494470590191741e-5
allele num: 120266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.23G>A
  hgvsp: ENSP00000450423.1:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.485G>A
  hgvsp: ENSP00000382806.2:p.Arg162Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.681G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.533G>A
  hgvsp: ENSP00000352956.3:p.Arg178Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.514G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.191G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.694G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.426G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.23G>A
  hgvsp: ENSP00000450556.1:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.431G>A
  hgvsp: ENSP00000339220.5:p.Arg144Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.23G>A
  hgvsp: ENSP00000452171.1:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-193G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.23G>A
  hgvsp: ENSP00000438504.2:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Arg178Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD

14-23374586-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374586
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374586
    reference: chr 14
allele count: 1
allele frequency: 8.315040244794785e-6
allele num: 120264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.484C>T
  hgvsp: ENSP00000382806.2:p.Arg162Trp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.680C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.532C>T
  hgvsp: ENSP00000352956.3:p.Arg178Trp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.22C>T
  hgvsp: ENSP00000450423.1:p.Arg8Trp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.22C>T
  hgvsp: ENSP00000450556.1:p.Arg8Trp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-194C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.190C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.22C>T
  hgvsp: ENSP00000452171.1:p.Arg8Trp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.693C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.513C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.22C>T
  hgvsp: ENSP00000438504.2:p.Arg8Trp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.425C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.430C>T
  hgvsp: ENSP00000339220.5:p.Arg144Trp
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5403
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg178Trp
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

14-23374591-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374591
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374591
    reference: chr 14
allele count: 2
allele frequency: 1.66281447978849e-5
allele num: 120278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-199G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.420G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.675G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.425G>A
  hgvsp: ENSP00000339220.5:p.Arg142Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.508G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.527G>A
  hgvsp: ENSP00000352956.3:p.Arg176Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.479G>A
  hgvsp: ENSP00000382806.2:p.Arg160Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.688G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.17G>A
  hgvsp: ENSP00000450556.1:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.17G>A
  hgvsp: ENSP00000450423.1:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.17G>A
  hgvsp: ENSP00000452171.1:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.185G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.17G>A
  hgvsp: ENSP00000438504.2:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg176Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

14-23374603-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374603
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374603
    reference: chr 14
allele count: 4
allele frequency: 3.324412825584681e-5
allele num: 120322
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.515A>T
  hgvsp: ENSP00000352956.3:p.Gln172Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-211A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.467A>T
  hgvsp: ENSP00000382806.2:p.Gln156Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.5A>T
  hgvsp: ENSP00000438504.2:p.Gln2Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.676A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.408A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.663A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.5A>T
  hgvsp: ENSP00000452171.1:p.Gln2Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.173A>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.413A>T
  hgvsp: ENSP00000339220.5:p.Gln138Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.5A>T
  hgvsp: ENSP00000450556.1:p.Gln2Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.5A>T
  hgvsp: ENSP00000450423.1:p.Gln2Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.496A>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5405
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln172Leu
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

14-23374617-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374617
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374617
    reference: chr 14
allele count: 6
allele frequency: 4.984796371068242e-5
allele num: 120366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.-10A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.501A>G
  hgvsp: ENST00000359890.3:c.501A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.453A>G
  hgvsp: ENST00000399922.2:c.453A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.159A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000555714
  gene symbol: RBM23
  hgvsc: ENST00000555714.1:n.549A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.394A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.482A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.399A>G
  hgvsp: ENST00000346528.5:c.399A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-225A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.662A>G
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.649A>G
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr167Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/14-23374621-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374621
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374621
    reference: chr 14
allele count: 1
allele frequency: 8.306613725848521e-6
allele num: 120386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.-14G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-229G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.645G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.658G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.449G>T
  hgvsp: ENSP00000382806.2:p.Arg150Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.478G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.497G>T
  hgvsp: ENSP00000352956.3:p.Arg166Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.-14G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.155G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.-14G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.395G>T
  hgvsp: ENSP00000339220.5:p.Arg132Leu
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.-14G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.390G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000555714
  gene symbol: RBM23
  hgvsc: ENST00000555714.1:n.545G>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg166Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

14-23374621-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374621
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374621
    reference: chr 14
allele count: 1
allele frequency: 8.306613725848521e-6
allele num: 120386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.478G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.155G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.-14G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.-14G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.658G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.-14G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.645G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.497G>C
  hgvsp: ENSP00000352956.3:p.Arg166Pro
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.395G>C
  hgvsp: ENSP00000339220.5:p.Arg132Pro
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.449G>C
  hgvsp: ENSP00000382806.2:p.Arg150Pro
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000555714
  gene symbol: RBM23
  hgvsc: ENST00000555714.1:n.545G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.390G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-229G>C
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.-14G>C
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg166Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

14-23374621-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374621
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374621
    reference: chr 14
allele count: 6
allele frequency: 4.983968235509113e-5
allele num: 120386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.449G>A
  hgvsp: ENSP00000382806.2:p.Arg150His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.-14G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.155G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.395G>A
  hgvsp: ENSP00000339220.5:p.Arg132His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.645G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-229G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000555714
  gene symbol: RBM23
  hgvsc: ENST00000555714.1:n.545G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.497G>A
  hgvsp: ENSP00000352956.3:p.Arg166His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.478G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.-14G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.390G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.-14G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.658G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.-14G>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg166His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

14-23374622-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374622
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374622
    reference: chr 14
allele count: 2
allele frequency: 1.661019201381968e-5
allele num: 120408
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.496C>T
  hgvsp: ENSP00000352956.3:p.Arg166Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.657C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.-15C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.154C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-230C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.644C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.-15C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.477C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.389C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.448C>T
  hgvsp: ENSP00000382806.2:p.Arg150Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.394C>T
  hgvsp: ENSP00000339220.5:p.Arg132Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.-15C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.-15C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000555714
  gene symbol: RBM23
  hgvsc: ENST00000555714.1:n.544C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg166Cys
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

14-23374630-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374630
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374630
    reference: chr 14
allele count: 3
allele frequency: 2.490949549968448e-5
allele num: 120436
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.386G>A
  hgvsp: ENSP00000339220.5:p.Arg129His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.-23G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.146G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.381G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.488G>A
  hgvsp: ENSP00000352956.3:p.Arg163His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-238G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.440G>A
  hgvsp: ENSP00000382806.2:p.Arg147His
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.-23G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.636G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.649G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.-23G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.469G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.-23G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000555714
  gene symbol: RBM23
  hgvsc: ENST00000555714.1:n.536G>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5406
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Arg163His
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

14-23374631-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374631
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374631
    reference: chr 14
allele count: 5
allele frequency: 4.150893272232185e-5
allele num: 120456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-239C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.-24C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.380C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.-24C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.439C>T
  hgvsp: ENSP00000382806.2:p.Arg147Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.468C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.487C>T
  hgvsp: ENSP00000352956.3:p.Arg163Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.385C>T
  hgvsp: ENSP00000339220.5:p.Arg129Cys
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.-24C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.648C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000555714
  gene symbol: RBM23
  hgvsc: ENST00000555714.1:n.535C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.-24C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.145C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.635C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5406
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg163Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-23374632-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374632
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374632
    reference: chr 14
allele count: 1
allele frequency: 8.301510874979247e-6
allele num: 120460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.-25G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.647G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452583
  ensembl transcript: ENST00000554256
  gene symbol: RBM23
  hgvsc: ENST00000554256.1:c.432G>T
  hgvsp: ENSP00000452583.1:p.Glu144Asp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-240G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.486G>T
  hgvsp: ENSP00000352956.3:p.Glu162Asp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.-25G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.384G>T
  hgvsp: ENSP00000339220.5:p.Glu128Asp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.438G>T
  hgvsp: ENSP00000382806.2:p.Glu146Asp
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.-25G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.379G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.634G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.-25G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.144G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000555714
  gene symbol: RBM23
  hgvsc: ENST00000555714.1:n.534G>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.467G>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu162Asp
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-23374644-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374644
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374645
    reference: chr 14
allele count: 1
allele frequency: 8.29462508294625e-6
allele num: 120560
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.634dupT
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.371dupT
  hgvsp: ENSP00000339220.5:p.Ser125GlufsTer3
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.473dupT
  hgvsp: ENSP00000352956.3:p.Ser159GlufsTer3
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.-38dupT
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-253dupT
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452583
  ensembl transcript: ENST00000554256
  gene symbol: RBM23
  hgvsc: ENST00000554256.1:c.419dupT
  hgvsp: ENSP00000452583.1:p.Ser141GlufsTer3
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.425dupT
  hgvsp: ENSP00000382806.2:p.Ser143GlufsTer3
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.-38dupT
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000555714
  gene symbol: RBM23
  hgvsc: ENST00000555714.1:n.521dupT
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.-38dupT
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.454dupT
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.366dupT
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.131dupT
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.-38dupT
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.621dupT
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser159GlufsTer3
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

14-23374658-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374658
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374658
    reference: chr 14
allele count: 30
allele frequency: 2.487273450843186e-4
allele num: 120614
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-266C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.441C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.460C>T
  hgvsp: ENSP00000352956.3:p.Pro154Ser
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.608C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.-51C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.118C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.358C>T
  hgvsp: ENSP00000339220.5:p.Pro120Ser
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.412C>T
  hgvsp: ENSP00000382806.2:p.Pro138Ser
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.621C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000555714
  gene symbol: RBM23
  hgvsc: ENST00000555714.1:n.508C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452583
  ensembl transcript: ENST00000554256
  gene symbol: RBM23
  hgvsc: ENST00000554256.1:c.406C>T
  hgvsp: ENSP00000452583.1:p.Pro136Ser
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.353C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5751
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro154Ser
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

14-23374663-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374663
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374663
    reference: chr 14
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000555714
  gene symbol: RBM23
  hgvsc: ENST00000555714.1:n.504-1G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.604-1G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.-55-1G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.354-1G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.-55-1G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.-55-1G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.437-1G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.349-1G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-270-1G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.456-1G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.-55-1G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.113G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452583
  ensembl transcript: ENST00000554256
  gene symbol: RBM23
  hgvsc: ENST00000554256.1:c.402-1G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.408-1G>A
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.617-1G>A
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: splice acceptor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.456-1G>A
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

14-23374670-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23374670
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23374670
    reference: chr 14
allele count: 1
allele frequency: 8.286926544683108e-6
allele num: 120672
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000352956
  ensembl transcript: ENST00000359890
  gene symbol: RBM23
  hgvsc: ENST00000359890.3:c.456-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000382806
  ensembl transcript: ENST00000399922
  gene symbol: RBM23
  hgvsc: ENST00000399922.2:c.408-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000339220
  ensembl transcript: ENST00000346528
  gene symbol: RBM23
  hgvsc: ENST00000346528.5:c.354-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452171
  ensembl transcript: ENST00000557403
  gene symbol: RBM23
  hgvsc: ENST00000557403.1:c.-55-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000556186
  gene symbol: RBM23
  hgvsc: ENST00000556186.1:n.106C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000555714
  gene symbol: RBM23
  hgvsc: ENST00000555714.1:n.504-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452583
  ensembl transcript: ENST00000554256
  gene symbol: RBM23
  hgvsc: ENST00000554256.1:c.402-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000452602
  ensembl transcript: ENST00000555209
  gene symbol: RBM23
  hgvsc: ENST00000555209.1:c.-270-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553920
  gene symbol: RBM23
  hgvsc: ENST00000553920.1:n.437-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000553738
  gene symbol: RBM23
  hgvsc: ENST00000553738.1:n.349-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000438504
  ensembl transcript: ENST00000542016
  gene symbol: RBM23
  hgvsc: ENST00000542016.2:c.-55-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450556
  ensembl transcript: ENST00000555722
  gene symbol: RBM23
  hgvsc: ENST00000555722.1:c.-55-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000307814
  gene symbol: RBM23
  hgvsc: ENST00000307814.6:n.617-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl protein: ENSP00000450423
  ensembl transcript: ENST00000557227
  gene symbol: RBM23
  hgvsc: ENST00000557227.1:c.-55-8C>T
  variant of: http://identifiers.org/hgnc/20155
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100461
  ensembl transcript: ENST00000557667
  gene symbol: RBM23
  hgvsc: ENST00000557667.1:n.604-8C>T
  variant of: http://identifiers.org/hgnc/20155
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2669
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.456-8C>T
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 1755
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1766
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2170
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4770
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1899
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45248
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.318571759795966e-4
allele num: 8626
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: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 3.309721e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.54e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.37e-1

QD
type: SiteQuality
SIO_000300: 1.279e1

GenotypeQuality
all individuals: 1756
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1899
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1770
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4779
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45243
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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: 898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.309467e6

VQSLOD
type: SiteQuality
SIO_000300: 6.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.69e-1

FS
type: SiteQuality
SIO_000300: 8.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.924e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.323e1

GenotypeQuality
all individuals: 1774
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 89
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1755
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4786
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1899
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45246
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1290
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.478e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.393e1

DP
type: SiteQuality
SIO_000300: 3.309393e6

FS
type: SiteQuality
SIO_000300: 1.9388e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4773
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1898
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45246
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQ
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ReadPosRankSum
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FS
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QD
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DP
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997512064986062e-5
allele num: 66722
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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MQRankSum
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ReadPosRankSum
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MQ
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FS
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BaseQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66714
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South Asian
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East Asian
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ClippingRankSum
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MQRankSum
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MQ
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BaseQRankSum
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FS
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InbreedingCoeff
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DP
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ReadPosRankSum
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QD
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VQSLOD
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SIO_000300: -8.02e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 2
allele frequency: 2.040399918384003e-4
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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FS
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MQ
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DP
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ClippingRankSum
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SIO_000300: -1.286e0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
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
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 2.318571759795966e-4
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ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQRankSum
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DP
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MQ
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

South Asian
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allele frequency: 1.211240310077519e-4
allele num: 16512
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QD
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FS
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DP
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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BaseQRankSum
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele num: 66716
num of homozygotes: 0

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

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

Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

South Asian
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African
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allele num: 9788
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.997871511227029e-5
allele num: 66714
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.992e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

QD
type: SiteQuality
SIO_000300: 1.328e1

FS
type: SiteQuality
SIO_000300: 4.928e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

MQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

DP
type: SiteQuality
SIO_000300: 3.308822e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

GenotypeQuality
all individuals: 45279
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.021659174499387e-4
allele num: 9788
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.092e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.74e0

VQSLOD
type: SiteQuality
SIO_000300: -1.09e0

DP
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SIO_000300: 3.309093e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

FS
type: SiteQuality
SIO_000300: 6.262e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.674e0

QD
type: SiteQuality
SIO_000300: 1.183e1

GenotypeQuality
all individuals: 320
bin: 7.25e1
variant carriers: 46

GenotypeQuality
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bin: 8.25e1
variant carriers: 119

GenotypeQuality
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bin: 2.75e1
variant carriers: 6

GenotypeQuality
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variant carriers: 13

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 8

GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 21

GenotypeQuality
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variant carriers: 14

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 47473

GenotypeQuality
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variant carriers: 105

GenotypeQuality
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variant carriers: 148

GenotypeQuality
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variant carriers: 27

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 17

GenotypeQuality
all individuals: 412
bin: 8.75e1
variant carriers: 106

European (Non-Finnish)
type: Population
allele count: 38239
allele frequency: 5.733843154895787e-1
allele num: 66690
num of homozygotes: 10958

Latino
type: Population
allele count: 7740
allele frequency: 6.693185748875822e-1
allele num: 11564
num of homozygotes: 2578

Other
type: Population
allele count: 538
allele frequency: 6.004464285714286e-1
allele num: 896
num of homozygotes: 156

European (Finnish)
type: Population
allele count: 3777
allele frequency: 5.715799031476998e-1
allele num: 6608
num of homozygotes: 1075

African
type: Population
allele count: 1156
allele frequency: 1.181762420772848e-1
allele num: 9782
num of homozygotes: 93

South Asian
type: Population
allele count: 11779
allele frequency: 7.136192899551678e-1
allele num: 16506
num of homozygotes: 4232

East Asian
type: Population
allele count: 6789
allele frequency: 7.877697841726619e-1
allele num: 8618
num of homozygotes: 2679

VQSLOD
type: SiteQuality
SIO_000300: 6.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.329999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.285e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 2.281e1

DP
type: SiteQuality
SIO_000300: 4.164454e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

GenotypeQuality
all individuals: 1007
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 956
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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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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1288
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 49536
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variant carriers: 1

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e0

MQRankSum
type: SiteQuality
SIO_000300: 6.71e-1

DP
type: SiteQuality
SIO_000300: 3.788221e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.452e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 6.109e0

VQSLOD
type: SiteQuality
SIO_000300: 6.879999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.368e1

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49533
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 140
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 80
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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
all individuals: 4
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1007
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1276
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
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: 896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.36e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

QD
type: SiteQuality
SIO_000300: 1.605e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.67e-2

DP
type: SiteQuality
SIO_000300: 3.786756e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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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: 45
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GenotypeQuality
all individuals: 954
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.455206691720208e-4
allele num: 16498
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.67e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

DP
type: SiteQuality
SIO_000300: 3.786756e6

QD
type: SiteQuality
SIO_000300: 1.605e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 53
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GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 3.069995906672124e-4
allele num: 9772
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
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: 8622
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MQ
type: SiteQuality
SIO_000300: 5.943e1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.9e-2

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 1.097e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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SIO_000300: 1.94e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 87
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GenotypeQuality
all individuals: 958
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GenotypeQuality
all individuals: 1502
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
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: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

DP
type: SiteQuality
SIO_000300: 3.785196e6

QD
type: SiteQuality
SIO_000300: 1.275e1

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 1252
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variant carriers: 0

GenotypeQuality
all individuals: 53
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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: 9.75e1
variant carriers: 10

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
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GenotypeQuality
all individuals: 1229
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.479471120389701e-4
allele num: 8622
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.05032560093629e-4
allele num: 66646
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.275e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

DP
type: SiteQuality
SIO_000300: 3.785196e6

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.75e1
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GenotypeQuality
all individuals: 1011
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.479471120389701e-4
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
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
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.784761e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

InbreedingCoeff
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SIO_000300: 9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.21e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

QD
type: SiteQuality
SIO_000300: 1.244e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1223
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.502070952638214e-5
allele num: 66636
num of homozygotes: 0

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

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

South Asian
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allele count: 4
allele frequency: 2.425418384671356e-4
allele num: 16492
num of homozygotes: 0

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

East Asian
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allele count: 10
allele frequency: 1.159823706796567e-3
allele num: 8622
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -1.121e0

QD
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SIO_000300: 1.355e1

FS
type: SiteQuality
SIO_000300: 1.094e0

MQRankSum
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SIO_000300: 3.15e-1

MQ
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SIO_000300: 5.963e1

DP
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SIO_000300: 3.784304e6

InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1365
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.819063788503517e-4
allele num: 16492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.024800163968026e-4
allele num: 9758
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

FS
type: SiteQuality
SIO_000300: 7.95e-1

BaseQRankSum
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SIO_000300: -8.34e-1

QD
type: SiteQuality
SIO_000300: 1.351e1

DP
type: SiteQuality
SIO_000300: 3.784061e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
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: 9744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66588
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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BaseQRankSum
type: SiteQuality
SIO_000300: -2.961e0

VQSLOD
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ClippingRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
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FS
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SIO_000300: 1.668e0

MQRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.122e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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: 16488
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.026272577996716e-4
allele num: 9744
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66594
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

QD
type: SiteQuality
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DP
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -2.119e0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 5
allele frequency: 5.132416341613632e-4
allele num: 9742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66574
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
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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East Asian
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allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

South Asian
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VQSLOD
type: SiteQuality
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MQ
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FS
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
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: 3
allele frequency: 1.820167455405897e-4
allele num: 16482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501997656883655e-5
allele num: 66578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 3.199e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-2

DP
type: SiteQuality
SIO_000300: 3.781269e6

QD
type: SiteQuality
SIO_000300: 1.455e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.09e-1

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

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 49514
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 136
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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: 16480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.081347576006573e-4
allele num: 9736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66560
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.121e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

DP
type: SiteQuality
SIO_000300: 3.780163e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.763e0

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

QD
type: SiteQuality
SIO_000300: 1.273e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.41e-1

GenotypeQuality
all individuals: 49513
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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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
all individuals: 1224
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 9.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.79e-1

QD
type: SiteQuality
SIO_000300: 1.244e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

DP
type: SiteQuality
SIO_000300: 3.780127e6

VQSLOD
type: SiteQuality
SIO_000300: 9.29e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.06e0

GenotypeQuality
all individuals: 1461
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 1013
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1227
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 289
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GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 1217
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variant carriers: 0

GenotypeQuality
all individuals: 63
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GenotypeQuality
all individuals: 1365
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variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49514
bin: 9.75e1
variant carriers: 2

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.359e0

FS
type: SiteQuality
SIO_000300: 4.309e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 3.779649e6

QD
type: SiteQuality
SIO_000300: 1.46e1

MQ
type: SiteQuality
SIO_000300: 5.978e1

MQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

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

GenotypeQuality
all individuals: 121
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 1364
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variant carriers: 0

GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 91
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variant carriers: 0

GenotypeQuality
all individuals: 36
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GenotypeQuality
all individuals: 93
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variant carriers: 0

GenotypeQuality
all individuals: 297
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variant carriers: 0

GenotypeQuality
all individuals: 2737
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variant carriers: 0

GenotypeQuality
all individuals: 78
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GenotypeQuality
all individuals: 1220
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variant carriers: 0

GenotypeQuality
all individuals: 1456
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variant carriers: 0

GenotypeQuality
all individuals: 933
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variant carriers: 0

GenotypeQuality
all individuals: 145
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GenotypeQuality
all individuals: 1230
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49516
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1013
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
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: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502674761074713e-5
allele num: 66548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.852e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.354e1

DP
type: SiteQuality
SIO_000300: 3.779376e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
all individuals: 1214
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503533303262667e-5
allele num: 66510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 3.778308e6

MQ
type: SiteQuality
SIO_000300: 5.897e1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: -1.191e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.608e0

FS
type: SiteQuality
SIO_000300: 1.207e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.09e-1

QD
type: SiteQuality
SIO_000300: 1.119e1

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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bin: 9.25e1
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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
all individuals: 1223
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GenotypeQuality
all individuals: 49517
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
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: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9708
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.102e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e-1

DP
type: SiteQuality
SIO_000300: 3.77833e6

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.272e1

FS
type: SiteQuality
SIO_000300: 8.534000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.393e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 1211
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.031140441328109e-4
allele num: 9698
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

QD
type: SiteQuality
SIO_000300: 1.335e1

VQSLOD
type: SiteQuality
SIO_000300: 4.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.447e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

FS
type: SiteQuality
SIO_000300: 3.915e0

DP
type: SiteQuality
SIO_000300: 3.778044e6

MQRankSum
type: SiteQuality
SIO_000300: 2.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.787e0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66488
num of homozygotes: 0

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

African
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allele count: 4
allele frequency: 4.126263668248401e-4
allele num: 9694
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

Other
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MQRankSum
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SIO_000300: -8.33e-1

ClippingRankSum
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SIO_000300: 3.36e-1

FS
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SIO_000300: 5.33e-1

ReadPosRankSum
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SIO_000300: -3.58e-1

MQ
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SIO_000300: 5.961e1

DP
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SIO_000300: 3.777603e6

BaseQRankSum
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SIO_000300: 2.42e0

QD
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SIO_000300: 1.652e1

VQSLOD
type: SiteQuality
SIO_000300: 6.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

GenotypeQuality
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variant carriers: 0

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

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

African
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allele frequency: 2.063131834124201e-4
allele num: 9694
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11548
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: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
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BaseQRankSum
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SIO_000300: 3.21e-1

MQRankSum
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SIO_000300: 1.07e-1

MQ
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SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 3.777387e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.58e-1

QD
type: SiteQuality
SIO_000300: 1.689e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.009419482981733e-5
allele num: 66458
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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Latino
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South Asian
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East Asian
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BaseQRankSum
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SIO_000300: 2.53e0

DP
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InbreedingCoeff
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ClippingRankSum
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MQ
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SIO_000300: 5.981e1

MQRankSum
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SIO_000300: 1.72e-1

VQSLOD
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SIO_000300: 1.5e-1

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: -1.078e0

QD
type: SiteQuality
SIO_000300: 1.507e1

GenotypeQuality
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variant carriers: 0

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

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

European (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: 2
allele frequency: 1.73190162798753e-4
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505026789476853e-5
allele num: 66444
num of homozygotes: 0

Other
type: Population
allele count: 0
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num of homozygotes: 0

African
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

DP
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 1.122e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 4
allele frequency: 2.426889940541196e-4
allele num: 16482
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 6
allele frequency: 9.031520004816811e-5
allele num: 66434
num of homozygotes: 0

Latino
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QD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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DP
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MQ
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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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GenotypeQuality
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GenotypeQuality
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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
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Latino
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allele count: 0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66422
num of homozygotes: 0

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

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

Latino
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allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505570611261668e-5
allele num: 66420
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

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

European (Non-Finnish)
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allele frequency: 3.011141222523336e-5
allele num: 66420
num of homozygotes: 0

African
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South Asian
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Other
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MQRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.162250116225012e-4
allele num: 8604
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.011322572874006e-5
allele num: 66416
num of homozygotes: 0

East Asian
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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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allele frequency: 0.0e0
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South Asian
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Other
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ReadPosRankSum
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DP
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VQSLOD
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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QD
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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variant carriers: 10

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 102
allele frequency: 1.535589545947248e-3
allele num: 66424
num of homozygotes: 0

South Asian
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allele count: 0
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African
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allele count: 1
allele frequency: 1.033698573495969e-4
allele num: 9674
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European (Finnish)
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allele count: 13
allele frequency: 1.966122202056866e-3
allele num: 6612
num of homozygotes: 0

Other
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allele count: 1
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allele num: 892
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MQ
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SIO_000300: 5.975e1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

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

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

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

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

Other
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QD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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FS
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DP
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 9

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

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: 5
allele frequency: 5.592841163310962e-3
allele num: 894
num of homozygotes: 1

African
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allele count: 285
allele frequency: 2.947259565667011e-2
allele num: 9670
num of homozygotes: 6

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

South Asian
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allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

Latino
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allele count: 18
allele frequency: 1.559251559251559e-3
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.515624059244988e-5
allele num: 66436
num of homozygotes: 0

VQSLOD
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MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 3.54e-2

FS
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SIO_000300: 5.23e-1

DP
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ClippingRankSum
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SIO_000300: -1.04e-1

QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 1.03476821192053e-4
allele num: 9664
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504845602841149e-5
allele num: 66452
num of homozygotes: 0

South Asian
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allele frequency: 1.820830298616169e-4
allele num: 16476
num of homozygotes: 0

Other
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BaseQRankSum
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VQSLOD
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DP
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ClippingRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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MQRankSum
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504664459825459e-5
allele num: 66460
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele num: 8604
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South Asian
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allele count: 0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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ReadPosRankSum
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FS
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SIO_000300: 1.994e0

VQSLOD
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SIO_000300: 4.9e-1

BaseQRankSum
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SIO_000300: 7.48e-1

DP
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SIO_000300: 3.788627e6

GenotypeDepth
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variant carriers: 0

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

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

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

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
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allele num: 66452
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East Asian
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European (Finnish)
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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FS
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QD
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GenotypeDepth
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variant carriers: 0

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

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

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

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

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

East Asian
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.009328919650918e-5
allele num: 66460
num of homozygotes: 0

African
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Other
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FS
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DP
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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MQ
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 6
allele frequency: 9.019030153624147e-5
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num of homozygotes: 0

East Asian
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Other
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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South Asian
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MQ
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FS
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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DP
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MQRankSum
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QD
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VQSLOD
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SIO_000300: 8.96e-1

InbreedingCoeff
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SIO_000300: 2.4e-3

GenotypeDepth
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variant carriers: 0

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

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

African
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allele frequency: 0.0e0
allele num: 9686
num of homozygotes: 0

South Asian
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allele count: 0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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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
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

Latino
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East Asian
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European (Non-Finnish)
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Other
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South Asian
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African
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InbreedingCoeff
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DP
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BaseQRankSum
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QD
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MQ
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FS
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 1

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

Latino
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European (Non-Finnish)
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allele num: 66570
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East Asian
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African
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Other
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European (Finnish)
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FS
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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QD
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VQSLOD
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MQ
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DP
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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East Asian
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Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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Other
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QD
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DP
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InbreedingCoeff
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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South Asian
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BaseQRankSum
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ClippingRankSum
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QD
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FS
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MQ
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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South Asian
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East Asian
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African
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European (Non-Finnish)
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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Other
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VQSLOD
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ClippingRankSum
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QD
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ReadPosRankSum
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DP
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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East Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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ClippingRankSum
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MQ
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FS
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QD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 9.25e1
variant carriers: 0