12-123001965-A-ATCTCGATTTCTTCCTCTCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123001965
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123001984
    reference: chr 12
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: ATCTCGATTTCTTCCTCTCT
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsp: ENSP00000346678.2:p.Ser89ArgfsTer8
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsp: ENSP00000343315.4:p.Ser78ArgfsTer8
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsp: ENSP00000444159.1:p.Ser68ArgfsTer8
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsp: ENSP00000446470.1:p.Val31GlufsTer?
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsp: ENSP00000330188.6:p.Ser137ArgfsTer8
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser137ArgfsTer8
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

12-123001966-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123001966
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123001966
    reference: chr 12
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.202G>A
  hgvsp: ENSP00000444159.1:p.Ser68Asn
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1451G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.233G>A
  hgvsp: ENSP00000343315.4:p.Ser78Asn
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.91G>A
  hgvsp: ENSP00000446470.1:p.Val31Ile
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2899G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*279G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.266G>A
  hgvsp: ENSP00000346678.2:p.Ser89Asn
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.536G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.410G>A
  hgvsp: ENSP00000330188.6:p.Ser137Asn
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*257G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*279G>A
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser137Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

12-123001969-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123001969
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123001969
    reference: chr 12
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.407G>A
  hgvsp: ENSP00000330188.6:p.Arg136His
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.263G>A
  hgvsp: ENSP00000346678.2:p.Arg88His
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.199G>A
  hgvsp: ENSP00000444159.1:p.Arg67His
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*276G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.230G>A
  hgvsp: ENSP00000343315.4:p.Arg77His
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*276G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1448G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*254G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.88G>A
  hgvsp: ENSP00000446470.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.533G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2896G>A
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg136His
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

12-123001970-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123001970
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123001970
    reference: chr 12
allele count: 2
allele frequency: 1.650192247396822e-5
allele num: 121198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*253C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.262C>T
  hgvsp: ENSP00000346678.2:p.Arg88Cys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.87C>T
  hgvsp: ENST00000526560.2:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.406C>T
  hgvsp: ENSP00000330188.6:p.Arg136Cys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.532C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2895C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*275C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.198C>T
  hgvsp: ENSP00000444159.1:p.Arg67Cys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*275C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1447C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.229C>T
  hgvsp: ENSP00000343315.4:p.Arg77Cys
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg136Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

12-123001976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123001976
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123001976
    reference: chr 12
allele count: 1
allele frequency: 8.258593066085262e-6
allele num: 121086
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.256C>T
  hgvsp: ENSP00000346678.2:p.Arg86Cys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2889C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.81C>T
  hgvsp: ENST00000526560.2:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.192C>T
  hgvsp: ENSP00000444159.1:p.Arg65Cys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*269C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*269C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.223C>T
  hgvsp: ENSP00000343315.4:p.Arg75Cys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.400C>T
  hgvsp: ENSP00000330188.6:p.Arg134Cys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1441C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*247C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.526C>T
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg134Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

12-123001988-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123001988
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123001988
    reference: chr 12
allele count: 1
allele frequency: 8.306889734345666e-6
allele num: 120382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.222-11T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.399-11T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.255-11T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*268-11T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.525-11T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.80-11T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.191-11T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1440-11T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2888-11T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*268-11T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*246-11T>A
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26504
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

12-123001994-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123001994
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123001994
    reference: chr 12
allele count: 1
allele frequency: 8.357290900581667e-6
allele num: 119656
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*268-17G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*246-17G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.525-17G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.80-17G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.255-17G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.399-17G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2888-17G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*268-17G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1440-17G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.222-17G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.191-17G>C
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

12-123001996-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123001996
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123001996
    reference: chr 12
allele count: 4
allele frequency: 3.351487222454964e-5
allele num: 119350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1440-19T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*246-19T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.191-19T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.399-19T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.255-19T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*268-19T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.525-19T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2888-19T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.80-19T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.222-19T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*268-19T>C
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6123
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

12-123001999-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123001999
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123001999
    reference: chr 12
allele count: 3
allele frequency: 2.519610972065913e-5
allele num: 119066
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.255-22A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2888-22A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.525-22A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.80-22A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*246-22A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*268-22A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1440-22A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.399-22A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.191-22A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.222-22A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*268-22A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6096
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10491
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

12-123002001-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123002001
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123002001
    reference: chr 12
allele count: 1
allele frequency: 8.402655239055541e-6
allele num: 119010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.80-24C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.525-24C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.222-24C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2888-24C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1440-24C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*268-24C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*268-24C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.399-24C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.191-24C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.255-24C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*246-24C>A
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

12-123002004-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123002004
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123002004
    reference: chr 12
allele count: 2
allele frequency: 1.683303314424226e-5
allele num: 118814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.525-27T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*246-27T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.80-27T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.222-27T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2888-27T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*268-27T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.191-27T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.255-27T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.399-27T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1440-27T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*268-27T>C
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21261
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

12-123002004-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123002004
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123002004
    reference: chr 12
allele count: 1
allele frequency: 8.41651657212113e-6
allele num: 118814
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.255-27T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.525-27T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1440-27T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.191-27T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2888-27T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.399-27T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*268-27T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*246-27T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.222-27T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.80-27T>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*268-27T>A
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-123002019-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123002019
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123002019
    reference: chr 12
allele count: 2
allele frequency: 1.707504482199266e-5
allele num: 117130
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.191-42A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.222-42A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*268-42A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.255-42A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*246-42A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*268-42A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.399-42A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.525-42A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1440-42A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2888-42A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.80-42A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9255
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7952
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: T
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

12-123002023-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123002023
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123002023
    reference: chr 12
allele count: 22
allele frequency: 1.892668490510848e-4
allele num: 116238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1440-46C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.525-46C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.255-46C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.399-46C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2888-46C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.80-46C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.191-46C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.222-46C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*268-46C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*246-46C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*268-46C>T
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9120
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10357
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9018
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14658
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-123002028-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123002028
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123002028
    reference: chr 12
allele count: 1
allele frequency: 8.722502311463112e-6
allele num: 114646
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.525-51T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.222-51T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.399-51T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*246-51T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1440-51T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.255-51T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*268-51T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.191-51T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*268-51T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2888-51T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.80-51T>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14456
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

12-123003341-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003341
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003341
    reference: chr 12
allele count: 1
allele frequency: 8.255047961828658e-6
allele num: 121138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2887+45A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*245+45A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.398+45A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.79+45A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.190+45A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1439+45A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*267+45A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.221+45A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.524+45A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*267+45A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.254+45A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

12-123003347-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003347
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003347
    reference: chr 12
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.254+39A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.221+39A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1439+39A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*245+39A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.190+39A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.398+39A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2887+39A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.79+39A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*267+39A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*267+39A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.524+39A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

12-123003349-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003349
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003349
    reference: chr 12
allele count: 3
allele frequency: 2.476432616268511e-5
allele num: 121142
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*267+37C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*267+37C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.79+37C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1439+37C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.221+37C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*245+37C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2887+37C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.524+37C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.398+37C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.254+37C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.190+37C>T
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27189
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

12-123003357-GTAC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003357
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003354
    reference: chr 12
allele count: 3
allele frequency: 2.475002475002475e-5
allele num: 121212
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.398+26_398+28delGTA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.190+26_190+28delGTA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1439+26_1439+28delGTA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2887+26_2887+28delGTA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.524+26_524+28delGTA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.221+26_221+28delGTA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*245+26_*245+28delGTA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.254+26_254+28delGTA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.79+26_79+28delGTA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*267+26_*267+28delGTA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*267+26_*267+28delGTA
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27344
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: GTAC
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

12-123003361-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003361
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003361
    reference: chr 12
allele count: 236
allele frequency: 1.946520182774946e-3
allele num: 121242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.524+25A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1439+25A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*267+25A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.398+25A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.254+25A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.79+25A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2887+25A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.190+25A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*245+25A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*267+25A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.221+25A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27450
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10194
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12199
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 9.75e1
  variant carriers: 209
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 4
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

12-123003364-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003364
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003364
    reference: chr 12
allele count: 2
allele frequency: 1.649076517150396e-5
allele num: 121280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.190+22T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.398+22T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*245+22T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1439+22T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.79+22T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*267+22T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2887+22T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.254+22T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.221+22T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.524+22T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*267+22T>C
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

12-123003366-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003366
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003366
    reference: chr 12
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1439+20A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.79+20A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*267+20A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*267+20A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.524+20A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*245+20A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2887+20A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.254+20A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.190+20A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.221+20A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.398+20A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

12-123003370-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003370
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003370
    reference: chr 12
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.254+16T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.190+16T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1439+16T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2887+16T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.398+16T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*245+16T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.524+16T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.221+16T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*267+16T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.79+16T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*267+16T>C
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-123003371-TACA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003371
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003368
    reference: chr 12
allele count: 15
allele frequency: 1.236623852000857e-4
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.398+12_398+14delTGT
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2887+12_2887+14delTGT
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.254+12_254+14delTGT
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.79+12_79+14delTGT
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*267+12_*267+14delTGT
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.221+12_221+14delTGT
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*267+12_*267+14delTGT
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1439+12_1439+14delTGT
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.190+12_190+14delTGT
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*245+12_*245+14delTGT
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.524+12_524+14delTGT
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: TACA
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/12-123003372-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003372
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003372
    reference: chr 12
allele count: 2
allele frequency: 1.64883180266781e-5
allele num: 121298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.79+14T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*267+14T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.524+14T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.398+14T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*267+14T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.254+14T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.221+14T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.190+14T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2887+14T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*245+14T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1439+14T>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

12-123003376-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003376
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003376
    reference: chr 12
allele count: 2
allele frequency: 1.648424106554134e-5
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*267+10G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2887+10G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*245+10G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.398+10G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.524+10G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*267+10G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.190+10G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.254+10G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.79+10G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.221+10G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1439+10G>A
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

12-123003388-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003388
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003388
    reference: chr 12
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2885A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*243A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*265A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.396A>C
  hgvsp: ENSP00000330188.6:p.Glu132Asp
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.188A>C
  hgvsp: ENSP00000444159.1:p.Glu63Asp
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.219A>C
  hgvsp: ENSP00000343315.4:p.Glu73Asp
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.77A>C
  hgvsp: ENSP00000446470.1:p.Lys26Thr
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1437A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.252A>C
  hgvsp: ENSP00000346678.2:p.Glu84Asp
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.522A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.710A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*265A>C
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu132Asp
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

12-123003392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003392
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003392
    reference: chr 12
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*261G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.706G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.215G>A
  hgvsp: ENSP00000343315.4:p.Arg72His
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.392G>A
  hgvsp: ENSP00000330188.6:p.Arg131His
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.184G>A
  hgvsp: ENSP00000444159.1:p.Arg62His
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.518G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.73G>A
  hgvsp: ENSP00000446470.1:p.Val25Met
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2881G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*261G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.248G>A
  hgvsp: ENSP00000346678.2:p.Arg83His
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*239G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1433G>A
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg131His
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-123003393-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003393
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003393
    reference: chr 12
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*260C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.214C>T
  hgvsp: ENSP00000343315.4:p.Arg72Cys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2880C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.517C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.183C>T
  hgvsp: ENSP00000444159.1:p.Arg62Cys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.391C>T
  hgvsp: ENSP00000330188.6:p.Arg131Cys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1432C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*238C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.705C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.72C>T
  hgvsp: ENST00000526560.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.247C>T
  hgvsp: ENSP00000346678.2:p.Arg83Cys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*260C>T
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg131Cys
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum

12-123003394-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003394
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003394
    reference: chr 12
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*259T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.516T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.213T>C
  hgvsp: ENST00000344591.4:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*259T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.704T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.71T>C
  hgvsp: ENSP00000446470.1:p.Leu24Pro
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.390T>C
  hgvsp: ENST00000331738.7:c.390T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.182T>C
  hgvsp: ENST00000528263.1:c.182T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.246T>C
  hgvsp: ENST00000354654.2:c.246T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2879T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*237T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1431T>C
  variant of: http://identifiers.org/hgnc/30559
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu24Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

12-123003403-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003403
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003403
    reference: chr 12
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.507A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.204A>G
  hgvsp: ENST00000344591.4:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*250A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.695A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.173A>G
  hgvsp: ENST00000528263.1:c.173A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.381A>G
  hgvsp: ENST00000331738.7:c.381A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.237A>G
  hgvsp: ENST00000354654.2:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1422A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.62A>G
  hgvsp: ENSP00000446470.1:p.Asp21Gly
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*228A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*250A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2870A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp21Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP

12-123003416-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003416
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003416
    reference: chr 12
allele count: 95
allele frequency: 7.825886384605245e-4
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.191G>A
  hgvsp: ENSP00000343315.4:p.Arg64Lys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2857G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.49G>A
  hgvsp: ENSP00000446470.1:p.Glu17Lys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.368G>A
  hgvsp: ENSP00000330188.6:p.Arg123Lys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.160G>A
  hgvsp: ENSP00000444159.1:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.224G>A
  hgvsp: ENSP00000346678.2:p.Arg75Lys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1409G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*237G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*237G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*215G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.494G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.682G>A
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 9.75e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg123Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

12-123003420-CTCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003420
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003417
    reference: chr 12
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.487_489delAGA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*230_*232delAGA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.153_155delAGA
  hgvsp: ENSP00000444159.1:p.Arg52del
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2850_2852delAGA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.361_363delAGA
  hgvsp: ENSP00000330188.6:p.Arg121del
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*208_*210delAGA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1402_1404delAGA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.184_186delAGA
  hgvsp: ENSP00000343315.4:p.Arg62del
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.42_44delAGA
  hgvsp: ENSP00000446470.1:p.Glu15del
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.675_677delAGA
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.217_219delAGA
  hgvsp: ENSP00000346678.2:p.Arg73del
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*230_*232delAGA
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg121del
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: CTCT
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

12-123003424-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003424
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003424
    reference: chr 12
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.360A>C
  hgvsp: ENST00000331738.7:c.360A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.486A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*229A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1401A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.152A>C
  hgvsp: ENST00000528263.1:c.152A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.183A>C
  hgvsp: ENST00000344591.4:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*229A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.674A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.216A>C
  hgvsp: ENST00000354654.2:c.216A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2849A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.41A>C
  hgvsp: ENSP00000446470.1:p.Gln14Pro
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*207A>C
  variant of: http://identifiers.org/hgnc/30559
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln14Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-123003433-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003433
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003433
    reference: chr 12
allele count: 3
allele frequency: 2.471291826614165e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*220A>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.174A>T
  hgvsp: ENSP00000343315.4:p.Arg58Ser
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*198A>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2840A>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.351A>T
  hgvsp: ENSP00000330188.6:p.Arg117Ser
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.665A>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*220A>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.207A>T
  hgvsp: ENSP00000346678.2:p.Arg69Ser
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1392A>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.32A>T
  hgvsp: ENSP00000446470.1:p.Glu11Val
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.477A>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.143A>T
  hgvsp: ENSP00000444159.1:p.Arg48Ser
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg117Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

12-123003442-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003442
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003442
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.656C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.134C>G
  hgvsp: ENST00000528263.1:c.134C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2831C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*211C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*189C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.23C>G
  hgvsp: ENSP00000446470.1:p.Ala8Gly
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1383C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.198C>G
  hgvsp: ENST00000354654.2:c.198C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*211C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.165C>G
  hgvsp: ENST00000344591.4:c.165C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.468C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.342C>G
  hgvsp: ENST00000331738.7:c.342C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala8Gly
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

12-123003443-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003443
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003443
    reference: chr 12
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*188G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.133G>A
  hgvsp: ENSP00000444159.1:p.Arg45His
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.197G>A
  hgvsp: ENSP00000346678.2:p.Arg66His
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.341G>A
  hgvsp: ENSP00000330188.6:p.Arg114His
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.467G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.22G>A
  hgvsp: ENSP00000446470.1:p.Ala8Thr
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.655G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2830G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*210G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.164G>A
  hgvsp: ENSP00000343315.4:p.Arg55His
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1382G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*210G>A
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg114His
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

12-123003450-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003450
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003450
    reference: chr 12
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*203C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.126C>T
  hgvsp: ENSP00000444159.1:p.His43Tyr
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1375C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2823C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.334C>T
  hgvsp: ENSP00000330188.6:p.His112Tyr
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*203C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.190C>T
  hgvsp: ENSP00000346678.2:p.His64Tyr
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.157C>T
  hgvsp: ENSP00000343315.4:p.His53Tyr
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.15C>T
  hgvsp: ENST00000526560.2:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*181C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.460C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.648C>T
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His112Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

12-123003461-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003461
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003461
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*170G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.146G>C
  hgvsp: ENSP00000343315.4:p.Gly49Ala
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.323G>C
  hgvsp: ENSP00000330188.6:p.Gly108Ala
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.637G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.4G>C
  hgvsp: ENSP00000446470.1:p.Val2Leu
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.179G>C
  hgvsp: ENSP00000346678.2:p.Gly60Ala
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*192G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2812G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.115G>C
  hgvsp: ENSP00000444159.1:p.Gly39Ala
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*192G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1364G>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.449G>C
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly108Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

12-123003475-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003475
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003475
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.165T>C
  hgvsp: ENST00000354654.2:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1350T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*178T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*178T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2798T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.623T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-11T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.435T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*156T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.101T>C
  hgvsp: ENST00000528263.1:c.101T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.132T>C
  hgvsp: ENST00000344591.4:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.309T>C
  hgvsp: ENST00000331738.7:c.309T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn103Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

12-123003480-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003480
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003480
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.127C>T
  hgvsp: ENST00000344591.4:c.127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1345C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*173C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.160C>T
  hgvsp: ENST00000354654.2:c.160C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*173C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*151C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.519C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-16C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.430C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.96C>T
  hgvsp: ENST00000528263.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.618C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2793C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.304C>T
  hgvsp: ENST00000331738.7:c.304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12337
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu102Leu
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: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

12-123003481-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003481
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003481
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.617A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.303A>G
  hgvsp: ENST00000331738.7:c.303A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.518A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2792A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*172A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1344A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.126A>G
  hgvsp: ENST00000344591.4:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.95A>G
  hgvsp: ENST00000528263.1:c.95A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-17A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*150A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.429A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*172A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.159A>G
  hgvsp: ENST00000354654.2:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg101Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/12-123003482-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003482
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003482
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.517G>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-18G>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.158G>T
  hgvsp: ENSP00000346678.2:p.Arg53Leu
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2791G>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*171G>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.302G>T
  hgvsp: ENSP00000330188.6:p.Arg101Leu
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.428G>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.94G>T
  hgvsp: ENSP00000444159.1:p.Arg32Leu
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.616G>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*171G>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.125G>T
  hgvsp: ENSP00000343315.4:p.Arg42Leu
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1343G>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*149G>T
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg101Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

12-123003484-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003484
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003484
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*169G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.515G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2789G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*147G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1341G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*169G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.426G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.123G>A
  hgvsp: ENST00000344591.4:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-20G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.156G>A
  hgvsp: ENST00000354654.2:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.614G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.300G>A
  hgvsp: ENST00000331738.7:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.92G>A
  hgvsp: ENST00000528263.1:c.92G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu100Glu
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

12-123003486-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003486
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003486
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*167G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.90G>A
  hgvsp: ENSP00000444159.1:p.Glu31Lys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.298G>A
  hgvsp: ENSP00000330188.6:p.Glu100Lys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*167G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*145G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2787G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.121G>A
  hgvsp: ENSP00000343315.4:p.Glu41Lys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.612G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.513G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.424G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.154G>A
  hgvsp: ENSP00000346678.2:p.Glu52Lys
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-22G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1339G>A
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu100Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

12-123003498-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003498
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003498
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.142G>A
  hgvsp: ENSP00000346678.2:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*133G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.109G>A
  hgvsp: ENSP00000343315.4:p.Asp37Asn
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2775G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.501G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.412G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.286G>A
  hgvsp: ENSP00000330188.6:p.Asp96Asn
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-34G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.600G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.78G>A
  hgvsp: ENSP00000444159.1:p.Asp27Asn
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*155G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1327G>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*155G>A
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp96Asn
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

12-123003500-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003500
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003500
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2773C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.140C>T
  hgvsp: ENSP00000346678.2:p.Ser47Phe
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-36C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*131C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.76C>T
  hgvsp: ENSP00000444159.1:p.Ser26Phe
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.410C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.107C>T
  hgvsp: ENSP00000343315.4:p.Ser36Phe
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.499C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*153C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.284C>T
  hgvsp: ENSP00000330188.6:p.Ser95Phe
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*153C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.598C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1325C>T
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser95Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

12-123003503-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003503
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003503
    reference: chr 12
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-39C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.496C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.595C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.104C>T
  hgvsp: ENSP00000343315.4:p.Ser35Phe
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1322C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*150C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*128C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2770C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.281C>T
  hgvsp: ENSP00000330188.6:p.Ser94Phe
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.73C>T
  hgvsp: ENSP00000444159.1:p.Ser25Phe
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.137C>T
  hgvsp: ENSP00000346678.2:p.Ser46Phe
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*150C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.407C>T
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser94Phe
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

12-123003503-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003503
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003503
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.73C>A
  hgvsp: ENSP00000444159.1:p.Ser25Tyr
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.496C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.104C>A
  hgvsp: ENSP00000343315.4:p.Ser35Tyr
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.137C>A
  hgvsp: ENSP00000346678.2:p.Ser46Tyr
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-39C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.595C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.281C>A
  hgvsp: ENSP00000330188.6:p.Ser94Tyr
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*128C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*150C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1322C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*150C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.407C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2770C>A
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser94Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

12-123003506-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003506
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003506
    reference: chr 12
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.101A>G
  hgvsp: ENSP00000343315.4:p.His34Arg
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.134A>G
  hgvsp: ENSP00000346678.2:p.His45Arg
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-42A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*125A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1319A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2767A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.592A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.278A>G
  hgvsp: ENSP00000330188.6:p.His93Arg
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*147A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.493A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.70A>G
  hgvsp: ENSP00000444159.1:p.His24Arg
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.404A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*147A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His93Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: QD

12-123003511-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003511
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003511
    reference: chr 12
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.65A>G
  hgvsp: ENST00000528263.1:c.65A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-47A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*142A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.96A>G
  hgvsp: ENST00000344591.4:c.96A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.488A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1314A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.273A>G
  hgvsp: ENST00000331738.7:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.129A>G
  hgvsp: ENST00000354654.2:c.129A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*120A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*142A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.587A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2762A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.399A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27913
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys91Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS

12-123003521-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003521
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003521
    reference: chr 12
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*110A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.55A>G
  hgvsp: ENSP00000444159.1:p.His19Arg
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*132A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.86A>G
  hgvsp: ENSP00000343315.4:p.His29Arg
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1304A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.263A>G
  hgvsp: ENSP00000330188.6:p.His88Arg
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.478A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-57A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*132A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.389A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.119A>G
  hgvsp: ENSP00000346678.2:p.His40Arg
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2752A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.577A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His88Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

12-123003521-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003521
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003521
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*132A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.55A>C
  hgvsp: ENSP00000444159.1:p.His19Pro
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.86A>C
  hgvsp: ENSP00000343315.4:p.His29Pro
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.119A>C
  hgvsp: ENSP00000346678.2:p.His40Pro
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-57A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*110A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.478A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.577A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2752A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.263A>C
  hgvsp: ENSP00000330188.6:p.His88Pro
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*132A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1304A>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.389A>C
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His88Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

12-123003522-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003522
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003522
    reference: chr 12
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.118C>A
  hgvsp: ENSP00000346678.2:p.His40Asn
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.576C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2751C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.85C>A
  hgvsp: ENSP00000343315.4:p.His29Asn
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*109C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1303C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.54C>A
  hgvsp: ENSP00000444159.1:p.His19Asn
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*131C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*131C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.262C>A
  hgvsp: ENSP00000330188.6:p.His88Asn
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.388C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-58C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.477C>A
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His88Asn
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

12-123003547-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003547
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003547
    reference: chr 12
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*106C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.60C>T
  hgvsp: ENST00000344591.4:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-83C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.93C>T
  hgvsp: ENST00000354654.2:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1278C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.237C>T
  hgvsp: ENST00000331738.7:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.363C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*84C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*106C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.551C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.452C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2726C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.29C>T
  hgvsp: ENST00000528263.1:c.29C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser79Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/12-123003553-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003553
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003553
    reference: chr 12
allele count: 2
allele frequency: 1.648342591524222e-5
allele num: 121334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.87T>G
  hgvsp: ENSP00000346678.2:p.Asp29Glu
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2720T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1272T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*100T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.54T>G
  hgvsp: ENSP00000343315.4:p.Asp18Glu
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.23T>G
  hgvsp: ENSP00000444159.1:p.Asp8Glu
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-89T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.545T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.231T>G
  hgvsp: ENSP00000330188.6:p.Asp77Glu
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*100T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.357T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*78T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.446T>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp77Glu
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

12-123003563-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003563
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003563
    reference: chr 12
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.77A>G
  hgvsp: ENSP00000346678.2:p.Glu26Gly
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.221A>G
  hgvsp: ENSP00000330188.6:p.Glu74Gly
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.13A>G
  hgvsp: ENSP00000444159.1:p.Glu5Gly
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*90A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*68A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-99A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.535A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*90A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2710A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.44A>G
  hgvsp: ENSP00000343315.4:p.Glu15Gly
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1262A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.347A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.436A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu74Gly
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

12-123003566-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003566
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003566
    reference: chr 12
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*87A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.433A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-102A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1259A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2707A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.218A>G
  hgvsp: ENSP00000330188.6:p.His73Arg
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.74A>G
  hgvsp: ENSP00000346678.2:p.His25Arg
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000444159
  ensembl transcript: ENST00000528263
  gene symbol: RSRC2
  hgvsc: ENST00000528263.1:c.10A>G
  hgvsp: ENSP00000444159.1:p.His4Arg
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.41A>G
  hgvsp: ENSP00000343315.4:p.His14Arg
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.532A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*65A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.344A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*87A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His73Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

12-123003583-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003583
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003583
    reference: chr 12
allele count: 1
allele frequency: 8.29228651508367e-6
allele num: 120594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.334-7A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.423-7A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-112-7A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*70A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1249-7A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.515A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.208-7A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.24A>G
  hgvsp: ENST00000344591.4:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*70A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2690A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.57A>G
  hgvsp: ENST00000354654.2:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*55-7A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.208-7A>G
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD

12-123003589-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003589
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003589
    reference: chr 12
allele count: 1
allele frequency: 8.32126749546491e-6
allele num: 120174
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.51C>G
  hgvsp: ENSP00000346678.2:p.Phe17Leu
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-112-13C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.423-13C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.334-13C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1249-13C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*64C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*55-13C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.509C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*64C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.18C>G
  hgvsp: ENSP00000343315.4:p.Phe6Leu
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2684C>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.208-13C>G
  variant of: http://identifiers.org/hgnc/30559
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe6Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

12-123003605-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003605
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003605
    reference: chr 12
allele count: 1
allele frequency: 8.514986376021799e-6
allele num: 117440
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.208-29C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1249-29C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*55-7C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.500-7C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*55-7C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.42-7C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.334-29C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*55-29C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-112-29C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.423-29C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.9-7C>A
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2668C>A
  variant of: http://identifiers.org/hgnc/30559
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*55-7C>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

12-123003606-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003606
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003606
    reference: chr 12
allele count: 1
allele frequency: 8.518032675173342e-6
allele num: 117398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.423-30C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*55-8C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-112-30C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.500-8C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.42-8C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.9-8C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*55-8C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.208-30C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1249-30C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.334-30C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2667C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*55-30C>T
  variant of: http://identifiers.org/hgnc/30559
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24679
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*55-8C>T
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ

12-123003615-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003615
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003615
    reference: chr 12
allele count: 1
allele frequency: 8.673327782403553e-6
allele num: 115296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*55-39C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.423-39C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*55-17C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*55-17C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.500-17C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1249-39C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.208-39C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-112-39C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2658C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.334-39C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.42-17C>T
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.9-17C>T
  variant of: http://identifiers.org/hgnc/30559
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21733
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

12-123003621-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003621
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003621
    reference: chr 12
allele count: 1
allele frequency: 8.745233847553084e-6
allele num: 114348
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.208-45T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*55-23T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2652T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.9-23T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.500-23T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*55-45T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.42-23T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1249-45T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-112-45T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.334-45T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.423-45T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*55-23T>C
  variant of: http://identifiers.org/hgnc/30559
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/12-123003622-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003622
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003622
    reference: chr 12
allele count: 1
allele frequency: 8.754880846071685e-6
allele num: 114222
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*55-24T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.208-46T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.423-46T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.334-46T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1249-46T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*55-46T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*55-24T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2651T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.500-24T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.9-24T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.42-24T>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-112-46T>G
  variant of: http://identifiers.org/hgnc/30559
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8535
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-123003622-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003622
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003622
    reference: chr 12
allele count: 1
allele frequency: 8.754880846071685e-6
allele num: 114222
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.500-24T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1249-46T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.334-46T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.423-46T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*55-46T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.208-46T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*55-24T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-112-46T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.42-24T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2651T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.9-24T>C
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*55-24T>C
  variant of: http://identifiers.org/hgnc/30559
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8535
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

12-123003632-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123003632
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123003632
    reference: chr 12
allele count: 1
allele frequency: 8.893157604539068e-6
allele num: 112446
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000436515
  ensembl transcript: ENST00000532695
  gene symbol: RSRC2
  hgvsc: ENST00000532695.1:c.*55-56A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527461
  gene symbol: RSRC2
  hgvsc: ENST00000527461.1:n.500-34A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000531639
  gene symbol: RSRC2
  hgvsc: ENST00000531639.1:n.423-56A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000525335
  gene symbol: RSRC2
  hgvsc: ENST00000525335.2:n.334-56A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000330188
  ensembl transcript: ENST00000331738
  gene symbol: RSRC2
  hgvsc: ENST00000331738.7:c.208-56A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527796
  gene symbol: RSRC2
  hgvsc: ENST00000527796.2:n.2641A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl transcript: ENST00000527173
  gene symbol: RSRC2
  hgvsc: ENST00000527173.2:n.1249-56A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000412148
  ensembl transcript: ENST00000433877
  gene symbol: RSRC2
  hgvsc: ENST00000433877.2:c.*55-34A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000343315
  ensembl transcript: ENST00000344591
  gene symbol: RSRC2
  hgvsc: ENST00000344591.4:c.9-34A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000432725
  ensembl transcript: ENST00000527399
  gene symbol: RSRC2
  hgvsc: ENST00000527399.3:c.*55-34A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000446470
  ensembl transcript: ENST00000526560
  gene symbol: RSRC2
  hgvsc: ENST00000526560.2:c.-112-56A>G
  variant of: http://identifiers.org/hgnc/30559
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111011
  ensembl protein: ENSP00000346678
  ensembl transcript: ENST00000354654
  gene symbol: RSRC2
  hgvsc: ENST00000354654.2:c.42-34A>G
  variant of: http://identifiers.org/hgnc/30559
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8514
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1954
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6989
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 724
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2295
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37313
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1599
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8477
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.396e-1

MQ
type: SiteQuality
SIO_000300: 5.351e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.222e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e0

MQRankSum
type: SiteQuality
SIO_000300: -4.164e0

FS
type: SiteQuality
SIO_000300: 7.491e0

DP
type: SiteQuality
SIO_000300: 1.979834e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.079e0

QD
type: SiteQuality
SIO_000300: 5.2e-1

GenotypeDepth
all individuals: 213
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1599
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2293
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6989
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8468
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 724
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1954
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.616e0

QD
type: SiteQuality
SIO_000300: 1.639e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.961e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.85e-1

DP
type: SiteQuality
SIO_000300: 1.97932e6

GenotypeDepth
all individuals: 671
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6993
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37252
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8467
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2287
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1155
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1598
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1949
bin: 7.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.944e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.57e0

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

FS
type: SiteQuality
SIO_000300: 3.256e0

QD
type: SiteQuality
SIO_000300: 1.28e1

VQSLOD
type: SiteQuality
SIO_000300: 3.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

DP
type: SiteQuality
SIO_000300: 1.978265e6

GenotypeDepth
all individuals: 1127
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 251
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 722
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37154
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6987
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2279
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8422
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.733402669440111e-4
allele num: 11538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.426e0

VQSLOD
type: SiteQuality
SIO_000300: -2.636e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.49e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

MQRankSum
type: SiteQuality
SIO_000300: 8.2e-1

DP
type: SiteQuality
SIO_000300: 1.976388e6

QD
type: SiteQuality
SIO_000300: 8.24e0

GenotypeDepth
all individuals: 114
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 255
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14389
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 719
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8372
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2255
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37022
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6978
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 386
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.515610791148833e-4
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66548
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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VQSLOD
type: SiteQuality
SIO_000300: -5.967e-1

ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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SIO_000300: 7.199999999999999e-2

DP
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QD
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MQ
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SIO_000300: 5.911e1

FS
type: SiteQuality
SIO_000300: 7.313e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.86e-1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511898642315019e-5
allele num: 66142
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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6564
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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InbreedingCoeff
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FS
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QD
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MQ
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DP
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -1.99e-1

VQSLOD
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SIO_000300: 1.83e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 9.761811792268645e-5
allele num: 10244
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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South Asian
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East Asian
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QD
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FS
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
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ClippingRankSum
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SIO_000300: -7.44e-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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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.577077993409007e-5
allele num: 65544
num of homozygotes: 0

Other
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European (Finnish)
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allele count: 1
allele frequency: 1.527650473571647e-4
allele num: 6546
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South Asian
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.71e-1

FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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DP
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VQSLOD
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 3.75e0

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: 3

GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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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 frequency: 3.059226627508566e-5
allele num: 65376
num of homozygotes: 0

European (Finnish)
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South Asian
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East Asian
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allele num: 8378
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MQRankSum
type: SiteQuality
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VQSLOD
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MQ
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SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.1835e1

InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 9.809691975671964e-5
allele num: 10194
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 904
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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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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European (Finnish)
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DP
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FS
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MQRankSum
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BaseQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Other
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African
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European (Non-Finnish)
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Latino
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European (Finnish)
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BaseQRankSum
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DP
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QD
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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Other
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Latino
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European (Finnish)
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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DP
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BaseQRankSum
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MQRankSum
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QD
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MQ
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FS
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ClippingRankSum
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SIO_000300: -1.038e0

ReadPosRankSum
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SIO_000300: 1.42e0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16228
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11080
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.232741617357002e-4
allele num: 8112
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.960159362549801e-5
allele num: 10040
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64296
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 894
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FS
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ClippingRankSum
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VQSLOD
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DP
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MQRankSum
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ReadPosRankSum
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SIO_000300: 1.89e0

BaseQRankSum
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SIO_000300: -2.78e-1

QD
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SIO_000300: 1.438e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8008
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.840677434530344e-5
allele num: 63770
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9964
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10972
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

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

South Asian
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allele count: 17
allele frequency: 1.050290374397628e-3
allele num: 16186
num of homozygotes: 0

DP
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MQRankSum
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MQ
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VQSLOD
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QD
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InbreedingCoeff
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SIO_000300: -2.4e-3

BaseQRankSum
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SIO_000300: -1.929e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 0.0e0

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

South Asian
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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: 1.5927624872579e-5
allele num: 62784
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10790
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

African
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

FS
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DP
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VQSLOD
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InbreedingCoeff
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SIO_000300: 2.5e-3

ReadPosRankSum
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SIO_000300: 1.16e-1

ClippingRankSum
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SIO_000300: -4.7e-2

MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 8.9e-1

QD
type: SiteQuality
SIO_000300: 1.382e1

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

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

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

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

African
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allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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BaseQRankSum
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SIO_000300: 6.1e-1

MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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DP
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QD
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MQ
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16356
num of homozygotes: 0

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

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

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

East Asian
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allele frequency: 1.15606936416185e-4
allele num: 8650
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InbreedingCoeff
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FS
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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DP
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ClippingRankSum
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MQRankSum
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QD
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.501260352898812e-5
allele num: 66648
num of homozygotes: 0

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

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

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

Other
type: Population
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num of homozygotes: 0

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

Latino
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allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

QD
type: SiteQuality
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ReadPosRankSum
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FS
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VQSLOD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2432
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1942
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7382
bin: 9.75e1
variant carriers: 231

GenotypeQuality
all individuals: 110
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1524
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 217
allele frequency: 2.088144726712856e-2
allele num: 10392
num of homozygotes: 4

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

Latino
type: Population
allele count: 10
allele frequency: 8.641548565502938e-4
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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.349770539008369e-4
allele num: 66678
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.14e-1

DP
type: SiteQuality
SIO_000300: 2.085907e6

QD
type: SiteQuality
SIO_000300: 1.628e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.28e0

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

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

GenotypeQuality
all individuals: 956
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37708
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1535
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7823
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7203
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 86
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
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: 16456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999220202747286e-5
allele num: 66684
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.955e1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.050569e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.395e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.319e0

VQSLOD
type: SiteQuality
SIO_000300: -4.007e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.41e-2

QD
type: SiteQuality
SIO_000300: 1.258e1

GenotypeQuality
all individuals: 37754
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1538
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7197
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7832
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1962
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2443
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
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: 16458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.69e0

DP
type: SiteQuality
SIO_000300: 2.050865e6

MQRankSum
type: SiteQuality
SIO_000300: -7.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

QD
type: SiteQuality
SIO_000300: 1.642e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.812e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: -1.564e-1

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7836
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 661
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7196
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1968
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37831
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2441
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1531
bin: 8.25e1
variant carriers: 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: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 6.86e0

MQRankSum
type: SiteQuality
SIO_000300: -1.68e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

DP
type: SiteQuality
SIO_000300: 2.051809e6

VQSLOD
type: SiteQuality
SIO_000300: 9.46e-1

QD
type: SiteQuality
SIO_000300: 1.614e1

FS
type: SiteQuality
SIO_000300: 2.827e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.139e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e0

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

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2442
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7833
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37841
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7195
bin: 9.75e1
variant carriers: 15

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

African
type: Population
allele count: 11
allele frequency: 1.058506543494996e-3
allele num: 10392
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: -7.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.76e-1

QD
type: SiteQuality
SIO_000300: 1.75e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.708e1

VQSLOD
type: SiteQuality
SIO_000300: 6.05e0

DP
type: SiteQuality
SIO_000300: 2.053269e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

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

GenotypeQuality
all individuals: 7845
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37873
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variant carriers: 0

GenotypeQuality
all individuals: 1966
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variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 55
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2454
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1538
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7186
bin: 9.75e1
variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99868058054456e-5
allele num: 66696
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: 10370
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.227e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.71e0

MQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

QD
type: SiteQuality
SIO_000300: 1.572e1

DP
type: SiteQuality
SIO_000300: 2.050394e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.32e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

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

GenotypeQuality
all individuals: 37920
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 959
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variant carriers: 0

GenotypeQuality
all individuals: 7184
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2442
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1536
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7847
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998320940273447e-5
allele num: 66704
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: 16482
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: 10392
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

MQ
type: SiteQuality
SIO_000300: 5.986e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.664e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.056e0

MQRankSum
type: SiteQuality
SIO_000300: -6.6e-2

FS
type: SiteQuality
SIO_000300: 6.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 2.052061e6

QD
type: SiteQuality
SIO_000300: 1.061e1

GenotypeDepth
all individuals: 213
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2040
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1497
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10246
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 268
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 342
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variant carriers: 0

GenotypeQuality
all individuals: 7857
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variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2436
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variant carriers: 0

GenotypeQuality
all individuals: 7180
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38049
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1529
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 658
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
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
allele num: 908
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 1.0e-4

DP
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MQ
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ClippingRankSum
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VQSLOD
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FS
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ReadPosRankSum
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QD
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BaseQRankSum
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SIO_000300: 7.36e0

MQRankSum
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SIO_000300: -8.0e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele num: 16504
num of homozygotes: 0

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

VQSLOD
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QD
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FS
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MQRankSum
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DP
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InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
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SIO_000300: 5.989e1

BaseQRankSum
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SIO_000300: -1.883e0

ClippingRankSum
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SIO_000300: -6.28e-1

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

Other
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num of homozygotes: 0

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

European (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 frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

QD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: -1.176e0

DP
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SIO_000300: 2.052728e6

FS
type: SiteQuality
SIO_000300: 9.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.12e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

MQ
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SIO_000300: 5.944e1

BaseQRankSum
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SIO_000300: 4.78e0

MQRankSum
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SIO_000300: -1.593e0

ClippingRankSum
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SIO_000300: -1.21e0

DP
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.777e-1

ReadPosRankSum
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SIO_000300: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.403e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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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num of homozygotes: 0

Other
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European (Non-Finnish)
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allele num: 66736
num of homozygotes: 0

African
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South Asian
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InbreedingCoeff
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MQRankSum
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QD
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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FS
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 95

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 3.848374061958822e-4
allele num: 10394
num of homozygotes: 0

East Asian
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Latino
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allele frequency: 3.369039391845197e-3
allele num: 11576
num of homozygotes: 0

South Asian
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allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
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allele count: 48
allele frequency: 7.192519779429394e-4
allele num: 66736
num of homozygotes: 0

Other
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allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

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

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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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66738
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Other
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South Asian
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Latino
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European (Finnish)
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East Asian
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FS
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ReadPosRankSum
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MQRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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QD
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MQ
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ClippingRankSum
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VQSLOD
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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)
type: Population
allele count: 1
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South Asian
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African
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Latino
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East Asian
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Other
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FS
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DP
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QD
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VQSLOD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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South Asian
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African
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Latino
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MQRankSum
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DP
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MQ
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BaseQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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MQ
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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FS
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DP
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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VQSLOD
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ClippingRankSum
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MQ
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QD
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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East Asian
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African
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South Asian
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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FS
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ClippingRankSum
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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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European (Non-Finnish)
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Latino
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African
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South Asian
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QD
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ReadPosRankSum
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MQ
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VQSLOD
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MQRankSum
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FS
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DP
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European (Non-Finnish)
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African
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MQ
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VQSLOD
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DP
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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VQSLOD
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GenotypeQuality
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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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Latino
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East Asian
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South Asian
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African
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MQ
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DP
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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European (Non-Finnish)
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ClippingRankSum
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FS
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MQ
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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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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European (Finnish)
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num of homozygotes: 0

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

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

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

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

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

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

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

African
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Other
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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DP
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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East Asian
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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DP
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FS
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MQ
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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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East Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Other
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South Asian
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MQ
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InbreedingCoeff
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MQRankSum
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DP
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QD
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BaseQRankSum
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FS
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VQSLOD
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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
all individuals: 725
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64336
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

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

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

South Asian
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allele count: 1
allele frequency: 6.184291898577613e-5
allele num: 16170
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

FS
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SIO_000300: 6.658e0

QD
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MQ
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SIO_000300: 6.0e1

DP
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SIO_000300: 1.928304e6

ClippingRankSum
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SIO_000300: -3.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10140
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8214
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.555113212241851e-5
allele num: 64304
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

South Asian
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MQRankSum
type: SiteQuality
SIO_000300: 5.17e-1

DP
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SIO_000300: 1.927221e6

ReadPosRankSum
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SIO_000300: 8.83e-1

BaseQRankSum
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SIO_000300: -3.55e0

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 3.0e-4

VQSLOD
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SIO_000300: 2.92e0

ClippingRankSum
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SIO_000300: -2.3e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

MQ
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GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10802
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.585640440173786e-5
allele num: 63066
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.12e-1

QD
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VQSLOD
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SIO_000300: 2.93e-1

MQ
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SIO_000300: 6.0e1

DP
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FS
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: -6.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 914
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10652
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: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15782
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.59877214299418e-5
allele num: 62548
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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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MQ
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SIO_000300: 5.977e1

ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.778705e6

VQSLOD
type: SiteQuality
SIO_000300: -7.609e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 6.341958396752917e-5
allele num: 15768
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62486
num of homozygotes: 0

Other
type: Population
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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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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10000
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Latino
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num of homozygotes: 0

East Asian
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.341958396752917e-5
allele num: 15768
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6514
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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num of homozygotes: 0

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

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