11-114310224-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310224
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310224
    reference: chr 11
allele count: 5
allele frequency: 4.73368299471721e-5
allele num: 105626
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.68T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.-27T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.-27T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.-27T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1154T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.15T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.8T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.-27T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.-27T>G
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13260
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25465
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2199
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6378
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 9.75e1
  variant carriers: 5
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

11-114310224-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310224
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310224
    reference: chr 11
allele count: 1
allele frequency: 9.46736598943442e-6
allele num: 105626
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.-27T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.-27T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.-27T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.-27T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.15T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.8T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.-27T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.68T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1154T>C
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25465
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4205
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2199
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

11-114310228-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310228
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310228
    reference: chr 11
allele count: 64
allele frequency: 6.042866584836182e-4
allele num: 105910
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.-23G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.-23G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.72G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.-23G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.-23G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.12G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1150G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.19G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.-23G>T
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26183
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6502
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13698
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34230
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2564
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1915
  bin: 3.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

11-114310229-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310229
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310229
    reference: chr 11
allele count: 66
allele frequency: 6.223831617064615e-4
allele num: 106044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.-22C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.-22C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.-22C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.-22C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.13C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.-22C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.73C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1149C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.20C>T
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13888
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5331
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26313
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6325
  bin: 1.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2484
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 9.75e1
  variant carriers: 64
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1762
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

11-114310230-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310230
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310230
    reference: chr 11
allele count: 5
allele frequency: 4.704642541259715e-5
allele num: 106278
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1148C>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.-21C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.-21C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.21C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.-21C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.-21C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.14C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.-21C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.74C>G
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14107
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26616
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1735
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6052
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

11-114310230-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310230
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310230
    reference: chr 11
allele count: 7
allele frequency: 6.586499557763602e-5
allele num: 106278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.-21C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.74C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.14C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1148C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.21C>T
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26616
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14107
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1735
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2367
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP

11-114310232-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310232
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310232
    reference: chr 11
allele count: 1
allele frequency: 9.375761780644678e-6
allele num: 106658
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.-19T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.-19T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1146T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.16T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.76T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.-19T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.23T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.-19T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.-19T>A
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2187
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

11-114310239-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310239
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310239
    reference: chr 11
allele count: 1
allele frequency: 9.286258195122857e-6
allele num: 107686
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.23T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.83T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.-12T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.30T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1139T>C
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5748
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1575
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

11-114310240-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310240
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310240
    reference: chr 11
allele count: 10
allele frequency: 9.267325264582136e-5
allele num: 107906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1138G>A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.84G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.-11G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.31G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.24G>A
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28881
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15240
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

11-114310241-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310241
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310241
    reference: chr 11
allele count: 2
allele frequency: 1.849728089970774e-5
allele num: 108124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.25G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.-10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.85G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.32G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1137G>A
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4933
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

11-114310254-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310254
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310254
    reference: chr 11
allele count: 1
allele frequency: 9.106638739641198e-6
allele num: 109810
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.4C>G
  hgvsp: ENSP00000265881.5:p.Leu2Val
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.4C>G
  hgvsp: ENSP00000440665.1:p.Leu2Val
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.98C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.4C>G
  hgvsp: ENSP00000443842.1:p.Leu2Val
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.4C>G
  hgvsp: ENSP00000442703.1:p.Leu2Val
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1124C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.4C>G
  hgvsp: ENSP00000442380.1:p.Leu2Val
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.4C>G
  hgvsp: ENSP00000437460.1:p.Leu2Val
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.38C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.45C>G
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30505
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu2Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD

11-114310257-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310257
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310257
    reference: chr 11
allele count: 1
allele frequency: 9.079518422342878e-6
allele num: 110138
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1121G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.7G>A
  hgvsp: ENSP00000440665.1:p.Gly3Ser
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.7G>A
  hgvsp: ENSP00000265881.5:p.Gly3Ser
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.7G>A
  hgvsp: ENSP00000437460.1:p.Gly3Ser
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.7G>A
  hgvsp: ENSP00000442703.1:p.Gly3Ser
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.7G>A
  hgvsp: ENSP00000443842.1:p.Gly3Ser
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.7G>A
  hgvsp: ENSP00000442380.1:p.Gly3Ser
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.41G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.101G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.48G>A
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1036
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly3Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

11-114310261-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310261
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310261
    reference: chr 11
allele count: 1
allele frequency: 9.091900934647416e-6
allele num: 109988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.11G>A
  hgvsp: ENSP00000440665.1:p.Gly4Asp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.11G>A
  hgvsp: ENSP00000443842.1:p.Gly4Asp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.11G>A
  hgvsp: ENSP00000265881.5:p.Gly4Asp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.105G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.52G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.11G>A
  hgvsp: ENSP00000442380.1:p.Gly4Asp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.11G>A
  hgvsp: ENSP00000437460.1:p.Gly4Asp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.11G>A
  hgvsp: ENSP00000442703.1:p.Gly4Asp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.45G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1117G>A
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly4Asp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-114310262-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310262
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310262
    reference: chr 11
allele count: 3
allele frequency: 2.715325295970457e-5
allele num: 110484
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.46C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.12C>G
  hgvsp: ENST00000539275.1:c.12C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.53C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.12C>G
  hgvsp: ENST00000541703.1:c.12C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.106C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.12C>G
  hgvsp: ENST00000544196.1:c.12C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1116C>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.12C>G
  hgvsp: ENST00000539754.1:c.12C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.12C>G
  hgvsp: ENST00000543131.1:c.12C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.12C>G
  hgvsp: ENST00000265881.5:c.12C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17195
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30423
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly4Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

11-114310269-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310269
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310269
    reference: chr 11
allele count: 1
allele frequency: 9.00284489898808e-6
allele num: 111076
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.53G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.19G>C
  hgvsp: ENSP00000442703.1:p.Gly7Arg
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.19G>C
  hgvsp: ENSP00000443842.1:p.Gly7Arg
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.19G>C
  hgvsp: ENSP00000440665.1:p.Gly7Arg
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1109G>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.19G>C
  hgvsp: ENSP00000265881.5:p.Gly7Arg
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.19G>C
  hgvsp: ENSP00000437460.1:p.Gly7Arg
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.2G>C
  hgvsp: ENSP00000441639.1:p.Gly2Arg
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.60G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.113G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.19G>C
  hgvsp: ENSP00000442380.1:p.Gly7Arg
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly7Arg
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

11-114310273-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310273
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310273
    reference: chr 11
allele count: 1
allele frequency: 8.991350320991206e-6
allele num: 111218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.23C>T
  hgvsp: ENSP00000442703.1:p.Ser8Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1105C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.23C>T
  hgvsp: ENSP00000443842.1:p.Ser8Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.57C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.23C>T
  hgvsp: ENSP00000437460.1:p.Ser8Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.23C>T
  hgvsp: ENSP00000440665.1:p.Ser8Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.23C>T
  hgvsp: ENSP00000442380.1:p.Ser8Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.23C>T
  hgvsp: ENSP00000265881.5:p.Ser8Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.6C>T
  hgvsp: ENSP00000441639.1:p.Ser3Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.117C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.64C>T
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17681
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser8Phe
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-114310278-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310278
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310278
    reference: chr 11
allele count: 1
allele frequency: 8.988279283813908e-6
allele num: 111256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.28C>A
  hgvsp: ENSP00000437460.1:p.Leu10Met
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.69C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.28C>A
  hgvsp: ENSP00000443842.1:p.Leu10Met
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.28C>A
  hgvsp: ENSP00000442380.1:p.Leu10Met
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.11C>A
  hgvsp: ENSP00000441639.1:p.Leu5Met
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.122C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.28C>A
  hgvsp: ENSP00000440665.1:p.Leu10Met
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1100C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.28C>A
  hgvsp: ENSP00000442703.1:p.Leu10Met
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.28C>A
  hgvsp: ENSP00000265881.5:p.Leu10Met
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.62C>A
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu10Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum

11-114310300-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310300
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310300
    reference: chr 11
allele count: 14
allele frequency: 1.288920805023108e-4
allele num: 108618
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.50G>A
  hgvsp: ENSP00000440665.1:p.Ser17Asn
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.50G>A
  hgvsp: ENSP00000442380.1:p.Ser17Asn
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.50G>A
  hgvsp: ENSP00000442703.1:p.Ser17Asn
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.84G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.50G>A
  hgvsp: ENSP00000265881.5:p.Ser17Asn
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.144G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.50G>A
  hgvsp: ENSP00000437460.1:p.Ser17Asn
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1078G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.91G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.33G>A
  hgvsp: ENSP00000441639.1:p.Ser12Asn
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.50G>A
  hgvsp: ENSP00000443842.1:p.Ser17Asn
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser17Asn
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

11-114310304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310304
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310304
    reference: chr 11
allele count: 1
allele frequency: 9.342825644187828e-6
allele num: 107034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.54C>T
  hgvsp: ENST00000543131.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.1C>T
  hgvsp: ENST00000539119.1:c.1C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.54C>T
  hgvsp: ENST00000539754.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.54C>T
  hgvsp: ENST00000544196.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.37C>T
  hgvsp: ENST00000538198.1:c.37C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.54C>T
  hgvsp: ENST00000539275.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.148C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.95C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.54C>T
  hgvsp: ENST00000265881.5:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.54C>T
  hgvsp: ENST00000541703.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1074C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.88C>T
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17604
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His18His
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

11-114310307-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310307
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310307
    reference: chr 11
allele count: 309
allele frequency: 2.893475166679152e-3
allele num: 106792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.57A>G
  hgvsp: ENST00000539754.1:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.40A>G
  hgvsp: ENST00000538198.1:c.40A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.98A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.57A>G
  hgvsp: ENST00000539275.1:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.4A>G
  hgvsp: ENST00000539119.1:c.4A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.57A>G
  hgvsp: ENST00000265881.5:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.91A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.57A>G
  hgvsp: ENST00000541703.1:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.57A>G
  hgvsp: ENST00000543131.1:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.151A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.57A>G
  hgvsp: ENST00000544196.1:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1071A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17593
  bin: 2.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 1.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 3.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 1.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6031
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 24820
  bin: 2.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly19Gly
num of homozygotes: 2
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

11-114310307-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310307
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310307
    reference: chr 11
allele count: 1
allele frequency: 9.363997303168776e-6
allele num: 106792
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.57A>T
  hgvsp: ENST00000539754.1:c.57A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.40A>T
  hgvsp: ENST00000538198.1:c.40A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.57A>T
  hgvsp: ENST00000265881.5:c.57A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.98A>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.4A>T
  hgvsp: ENST00000539119.1:c.4A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.57A>T
  hgvsp: ENST00000544196.1:c.57A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.57A>T
  hgvsp: ENST00000543131.1:c.57A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.57A>T
  hgvsp: ENST00000541703.1:c.57A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1071A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.151A>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.91A>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.57A>T
  hgvsp: ENST00000539275.1:c.57A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24820
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly19Gly
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

11-114310308-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310308
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310307
    reference: chr 11
allele count: 3
allele frequency: 2.83077619883372e-5
allele num: 105978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.60delG
  hgvsp: ENSP00000442380.1:p.Phe21SerfsTer34
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.60delG
  hgvsp: ENSP00000442703.1:p.Phe21SerfsTer30
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.7delG
  hgvsp: ENSP00000444421.1:p.Phe4SerfsTer33
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.60delG
  hgvsp: ENSP00000440665.1:p.Phe21SerfsTer30
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.154delG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.94delG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.60delG
  hgvsp: ENSP00000443842.1:p.Phe21SerfsTer30
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.60delG
  hgvsp: ENSP00000437460.1:p.Phe21SerfsTer30
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.60delG
  hgvsp: ENSP00000265881.5:p.Phe21SerfsTer30
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.101delG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.43delG
  hgvsp: ENSP00000441639.1:p.Phe16SerfsTer30
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1068delG
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24170
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Phe21SerfsTer30
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: CG
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum

11-114310330-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310330
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310330
    reference: chr 11
allele count: 1
allele frequency: 1.075222571072212e-5
allele num: 93004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.80G>A
  hgvsp: ENSP00000437460.1:p.Arg27His
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.80G>A
  hgvsp: ENSP00000442703.1:p.Arg27His
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.80G>A
  hgvsp: ENSP00000443842.1:p.Arg27His
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.80G>A
  hgvsp: ENSP00000440665.1:p.Arg27His
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.80G>A
  hgvsp: ENSP00000265881.5:p.Arg27His
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.27G>A
  hgvsp: ENSP00000444421.1:p.Arg10His
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.174G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.63G>A
  hgvsp: ENSP00000441639.1:p.Arg22His
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.80G>A
  hgvsp: ENSP00000442380.1:p.Arg27His
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.114G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.121G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1048G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15527
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg27His
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

11-114310331-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310331
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310331
    reference: chr 11
allele count: 1
allele frequency: 1.075685211479713e-5
allele num: 92964
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.122C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.64C>G
  hgvsp: ENST00000538198.1:c.64C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.81C>G
  hgvsp: ENST00000539275.1:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.175C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1047C>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.81C>G
  hgvsp: ENST00000543131.1:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.81C>G
  hgvsp: ENST00000265881.5:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.115C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.28C>G
  hgvsp: ENST00000539119.1:c.28C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.81C>G
  hgvsp: ENST00000544196.1:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.81C>G
  hgvsp: ENST00000539754.1:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.81C>G
  hgvsp: ENST00000541703.1:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11065
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12094
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg27Arg
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

11-114310340-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310340
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310340
    reference: chr 11
allele count: 5
allele frequency: 5.724884929812911e-5
allele num: 87338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.90C>T
  hgvsp: ENST00000544196.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.124C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.90C>T
  hgvsp: ENST00000541703.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.90C>T
  hgvsp: ENST00000543131.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.184C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.73C>T
  hgvsp: ENST00000538198.1:c.73C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.90C>T
  hgvsp: ENST00000539754.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1038C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.37C>T
  hgvsp: ENST00000539119.1:c.37C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.131C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.90C>T
  hgvsp: ENST00000265881.5:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.90C>T
  hgvsp: ENST00000539275.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12885
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly30Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-114310345-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310345
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310345
    reference: chr 11
allele count: 351
allele frequency: 4.239847317179233e-3
allele num: 82786
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.95C>T
  hgvsp: ENSP00000265881.5:p.Ala32Val
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.42C>T
  hgvsp: ENSP00000444421.1:p.Ala15Val
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.95C>T
  hgvsp: ENSP00000442380.1:p.Ala32Val
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.78C>T
  hgvsp: ENSP00000441639.1:p.Ala27Val
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.95C>T
  hgvsp: ENSP00000443842.1:p.Ala32Val
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.95C>T
  hgvsp: ENSP00000437460.1:p.Ala32Val
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.136C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1033C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.95C>T
  hgvsp: ENSP00000440665.1:p.Ala32Val
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.189C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.129C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.95C>T
  hgvsp: ENSP00000442703.1:p.Ala32Val
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10776
  bin: 2.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 3.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14862
  bin: 1.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 1.75e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16375
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 9693
  bin: 2.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Ala32Val
num of homozygotes: 1
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

11-114310351-C-CCAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310351
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310354
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 77768
alternate allele: CCAT
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.101_102insCAT
  hgvsp: ENSP00000443842.1:p.Ala34_Ala35insMet
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.142_143insCAT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.84_85insCAT
  hgvsp: ENSP00000441639.1:p.Ala29_Ala30insMet
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.135_136insCAT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.101_102insCAT
  hgvsp: ENSP00000442380.1:p.Ala34_Ala35insMet
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.101_102insCAT
  hgvsp: ENSP00000265881.5:p.Ala34_Ala35insMet
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.48_49insCAT
  hgvsp: ENSP00000444421.1:p.Ala17_Ala18insMet
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.101_102insCAT
  hgvsp: ENSP00000437460.1:p.Ala34_Ala35insMet
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.101_102insCAT
  hgvsp: ENSP00000440665.1:p.Ala34_Ala35insMet
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.195_196insCAT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1027_*123-1026insCAT
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.101_102insCAT
  hgvsp: ENSP00000442703.1:p.Ala34_Ala35insMet
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: inframe insertion
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18265
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala34_Ala35insMet
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/11-114310354-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310354
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310354
    reference: chr 11
allele count: 2
allele frequency: 2.696144513345915e-5
allele num: 74180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.104C>A
  hgvsp: ENSP00000442703.1:p.Ala35Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.104C>A
  hgvsp: ENSP00000443842.1:p.Ala35Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.104C>A
  hgvsp: ENSP00000442380.1:p.Ala35Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.145C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.87C>A
  hgvsp: ENSP00000441639.1:p.Ala30Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.104C>A
  hgvsp: ENSP00000437460.1:p.Ala35Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.198C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.51C>A
  hgvsp: ENSP00000444421.1:p.Ala18Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.104C>A
  hgvsp: ENSP00000440665.1:p.Ala35Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.104C>A
  hgvsp: ENSP00000265881.5:p.Ala35Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.138C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1024C>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19631
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17123
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala35Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum

11-114310357-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310357
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310357
    reference: chr 11
allele count: 12
allele frequency: 1.677289500167729e-4
allele num: 71544
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.148G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.90G>A
  hgvsp: ENSP00000441639.1:p.Gly31Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.141G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.107G>A
  hgvsp: ENSP00000440665.1:p.Gly36Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.54G>A
  hgvsp: ENSP00000444421.1:p.Gly19Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.107G>A
  hgvsp: ENSP00000443842.1:p.Gly36Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.107G>A
  hgvsp: ENSP00000442703.1:p.Gly36Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.107G>A
  hgvsp: ENSP00000442380.1:p.Gly36Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.107G>A
  hgvsp: ENSP00000437460.1:p.Gly36Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.107G>A
  hgvsp: ENSP00000265881.5:p.Gly36Glu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1021G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.201G>A
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17694
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20465
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7068
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly36Glu
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/11-114310360-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310360
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310360
    reference: chr 11
allele count: 1
allele frequency: 1.416189882739478e-5
allele num: 70612
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.204A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.110A>C
  hgvsp: ENSP00000440665.1:p.Glu37Ala
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1018A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.151A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.57A>C
  hgvsp: ENSP00000444421.1:p.Glu20Ala
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.144A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.110A>C
  hgvsp: ENSP00000442380.1:p.Glu37Ala
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.93A>C
  hgvsp: ENSP00000441639.1:p.Glu32Ala
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.110A>C
  hgvsp: ENSP00000442703.1:p.Glu37Ala
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.110A>C
  hgvsp: ENSP00000265881.5:p.Glu37Ala
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.110A>C
  hgvsp: ENSP00000443842.1:p.Glu37Ala
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.110A>C
  hgvsp: ENSP00000437460.1:p.Glu37Ala
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20950
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17793
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu37Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

11-114310374-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310374
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310374
    reference: chr 11
allele count: 1
allele frequency: 1.71291538198013e-5
allele num: 58380
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-1004C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.107C>T
  hgvsp: ENSP00000441639.1:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.71C>T
  hgvsp: ENSP00000444421.1:p.Arg25Trp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.124C>T
  hgvsp: ENSP00000442380.1:p.Arg42Trp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.124C>T
  hgvsp: ENSP00000443842.1:p.Arg42Trp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.124C>T
  hgvsp: ENSP00000265881.5:p.Arg42Trp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.158C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.218C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.124C>T
  hgvsp: ENSP00000442703.1:p.Arg42Trp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.124C>T
  hgvsp: ENSP00000440665.1:p.Arg42Trp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.124C>T
  hgvsp: ENSP00000437460.1:p.Arg42Trp
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.165C>T
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23481
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6657
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg42Trp
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-114310379-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310379
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310379
    reference: chr 11
allele count: 32
allele frequency: 5.962584780502348e-4
allele num: 53668
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-999G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.129G>A
  hgvsp: ENSP00000442380.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.129G>A
  hgvsp: ENSP00000265881.5:p.Met43Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.163G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.76G>A
  hgvsp: ENSP00000444421.1:p.Met26Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.129G>A
  hgvsp: ENSP00000443842.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.129G>A
  hgvsp: ENSP00000437460.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.129G>A
  hgvsp: ENSP00000440665.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.112G>A
  hgvsp: ENSP00000441639.1:p.Met38Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.223G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.129G>A
  hgvsp: ENSP00000442703.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.170G>A
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18011
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8487
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24096
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Met43Ile
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

11-114310382-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310382
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310382
    reference: chr 11
allele count: 80
allele frequency: 1.641092967916633e-3
allele num: 48748
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.173C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.115C>T
  hgvsp: ENST00000538198.1:c.115C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.79C>T
  hgvsp: ENST00000539119.1:c.79C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.132C>T
  hgvsp: ENST00000539275.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-996C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.132C>T
  hgvsp: ENST00000543131.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.132C>T
  hgvsp: ENST00000539754.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.132C>T
  hgvsp: ENST00000541703.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.166C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.132C>T
  hgvsp: ENST00000265881.5:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.132C>T
  hgvsp: ENST00000544196.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.226C>T
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17168
  bin: 1.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 1.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10350
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24151
  bin: 7.5e0
  variant carriers: 21
genotype quality: GenotypeQuality
hgvs: p.Val44Val
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

11-114310391-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310391
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310391
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 44056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.175C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.141C>T
  hgvsp: ENST00000265881.5:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.141C>T
  hgvsp: ENST00000541703.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.141C>T
  hgvsp: ENST00000543131.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.141C>T
  hgvsp: ENST00000539275.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.124C>T
  hgvsp: ENST00000538198.1:c.124C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.235C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-987C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.141C>T
  hgvsp: ENST00000544196.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.88C>T
  hgvsp: ENST00000539119.1:c.88C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.182C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.141C>T
  hgvsp: ENST00000539754.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 15818
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24534
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp47Asp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-114310402-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310402
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310402
    reference: chr 11
allele count: 5
allele frequency: 1.47197362223269e-4
allele num: 33968
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.181+5G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.241+5G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.147+5G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.147+5G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.147+5G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.147+5G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+5G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.130+5G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.147+5G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.188+5G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+5G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-976G>C
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19321
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22390
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12493
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.147+5G>C
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

11-114310407-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310407
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310407
    reference: chr 11
allele count: 2
allele frequency: 7.124029351000925e-5
allele num: 28074
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.188+10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.130+10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.181+10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.241+10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.147+10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.147+10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-971G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.147+10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.147+10G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.147+10G>A
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20992
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23070
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-114310409-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310409
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310409
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 26106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.181+12C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+12C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.241+12C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.147+12C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.147+12C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.130+12C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.147+12C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.147+12C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-969C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.147+12C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.188+12C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+12C>A
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 20698
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

11-114310414-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310414
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310414
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 21038
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.147+17G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.241+17G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.147+17G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.181+17G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-964G>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.147+17G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.130+17G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.188+17G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.147+17G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+17G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+17G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.147+17G>C
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 27783
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18851
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

11-114310428-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310428
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310428
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 13874
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.147+31G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-950G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.147+31G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.241+31G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.181+31G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.147+31G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+31G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.147+31G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.130+31G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.188+31G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.147+31G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+31G>C
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 32163
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16879
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

11-114310429-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310429
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310429
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 13448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.147+32C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.147+32C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.241+32C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.147+32C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.181+32C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.147+32C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.130+32C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.188+32C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.147+32C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+32C>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-949C>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+32C>G
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16794
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

11-114310434-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310434
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310434
    reference: chr 11
allele count: 1
allele frequency: 8.163265306122449e-5
allele num: 12250
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.188+37G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+37G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+37G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.241+37G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.147+37G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.181+37G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.147+37G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-944G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.147+37G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.147+37G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.147+37G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.130+37G>A
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32850
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

11-114310439-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310439
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310439
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 11294
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.147+42T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-939T>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+42T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.147+42T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.147+42T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.130+42T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+42T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.188+42T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.241+42T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.181+42T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.147+42T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.147+42T>G
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16132
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32735
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

11-114310444-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310444
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310444
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 10494
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+47T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.147+47T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.188+47T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.147+47T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.130+47T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.241+47T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.147+47T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.181+47T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.147+47T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.147+47T>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-934T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+47T>A
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16157
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32605
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-114310817-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310817
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310817
    reference: chr 11
allele count: 1
allele frequency: 9.752291788570315e-5
allele num: 10254
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.147+420A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.147+420A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.147+420A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.27+308A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.147+420A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-561A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.188+420A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.241+420A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.147+420A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.130+420A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.181+420A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+420A>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+420A>C
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

11-114310817-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310817
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310817
    reference: chr 11
allele count: 2
allele frequency: 1.950458357714063e-4
allele num: 10254
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+420A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.147+420A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.147+420A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.181+420A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.241+420A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.147+420A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.130+420A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.147+420A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.27+308A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.147+420A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+420A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.188+420A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-561A>G
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

11-114310818-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310818
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310818
    reference: chr 11
allele count: 1
allele frequency: 9.738994935722633e-5
allele num: 10268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.188+421T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+421T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.130+421T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+421T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.241+421T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.181+421T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.147+421T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.147+421T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.147+421T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.27+309T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.147+421T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-560T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.147+421T>C
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

11-114310822-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310822
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310822
    reference: chr 11
allele count: 20
allele frequency: 1.940617116242965e-3
allele num: 10306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.241+425A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+425A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.188+425A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.147+425A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.147+425A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.147+425A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.147+425A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.147+425A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.130+425A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.181+425A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.27+313A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-556A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+425A>G
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/11-114310913-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310913
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310913
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 10192
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-465C>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+516C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.148-465C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.242-465C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.27+404C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+516C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.131-465C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.148-465C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.148-465C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.148-465C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.148-465C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.182-465C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.26+45C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.189-465C>A
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

11-114310914-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114310914
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114310914
    reference: chr 11
allele count: 1
allele frequency: 9.792401096748923e-5
allele num: 10212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.189-464C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.26+46C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.148-464C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.131-464C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.27+405C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.242-464C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.182-464C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.148-464C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-464C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.148-464C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.148-464C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.148-464C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+517C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+517C>T
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-114311331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311331
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311331
    reference: chr 11
allele count: 10
allele frequency: 8.383635144198524e-5
allele num: 119280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.27-47C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.242-47C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.148-47C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.28-47C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.131-47C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.182-47C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-47C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.148-47C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.148-47C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.148-47C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+934C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+934C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.148-47C>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.189-47C>T
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8403
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7592
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-114311332-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311332
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311332
    reference: chr 11
allele count: 1
allele frequency: 8.382510729613734e-6
allele num: 119296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+935C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.148-46C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.28-46C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.182-46C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.148-46C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.131-46C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.189-46C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+935C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.148-46C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.27-46C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.242-46C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.148-46C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.148-46C>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-46C>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7850
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

11-114311334-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311334
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311334
    reference: chr 11
allele count: 1
allele frequency: 8.372124175345769e-6
allele num: 119444
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.182-44G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+937G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.148-44G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.148-44G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.27-44G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.131-44G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+937G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.148-44G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.189-44G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.242-44G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.148-44G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.28-44G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.148-44G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-44G>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9799
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

11-114311337-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311337
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311337
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 119618
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.242-41T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.148-41T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.28-41T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.148-41T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.148-41T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.27-41T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+940T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.148-41T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.189-41T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.131-41T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.182-41T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.148-41T>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-41T>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+940T>G
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

11-114311347-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311347
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311347
    reference: chr 11
allele count: 1
allele frequency: 8.349057391420508e-6
allele num: 119774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+950G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.131-31G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.182-31G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.148-31G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.148-31G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.148-31G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.148-31G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.189-31G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.27-31G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-31G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.148-31G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.242-31G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.28-31G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+950G>T
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8468
  bin: 3.75e1
  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: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

11-114311357-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311357
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311357
    reference: chr 11
allele count: 4
allele frequency: 3.332278111931222e-5
allele num: 120038
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.148-21T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.148-21T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.148-21T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+960T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.242-21T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.28-21T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+960T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.148-21T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.148-21T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.189-21T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.27-21T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-21T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.131-21T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.182-21T>C
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

11-114311364-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311364
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311363
    reference: chr 11
allele count: 23
allele frequency: 1.912586482171368e-4
allele num: 120256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.148-9delT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.242-9delT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.148-9delT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.189-9delT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.28-9delT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.27-9delT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.148-9delT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+972delT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.148-9delT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+972delT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.182-9delT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-9delT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.131-9delT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.148-9delT
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: AT
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

11-114311365-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311365
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311365
    reference: chr 11
allele count: 1
allele frequency: 8.317945134833891e-6
allele num: 120222
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.242-13T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.28-13T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+968T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.27-13T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+968T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.182-13T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.131-13T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.148-13T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.148-13T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.148-13T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.148-13T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-13T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.189-13T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.148-13T>C
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

11-114311373-TGCAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311373
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311369
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 120466
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.148-4_148-1delGCAG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.148-4_148-1delGCAG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.242-4_242-1delGCAG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.182-4_182-1delGCAG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.148-4_148-1delGCAG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.131-4_131-1delGCAG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+977_94+980delGCAG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.28-4_28-1delGCAG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-4_*123-1delGCAG
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.148-4_148-1delGCAG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+977_147+980delGCAG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.189-4_189-1delGCAG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.27-4_27-1delGCAG
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.148-4_148-1delGCAG
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: splice acceptor
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 11051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.*123-4_*123-1delGCAG
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
reference allele: TGCAG
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD

11-114311374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311374
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311374
    reference: chr 11
allele count: 4
allele frequency: 3.320494089520521e-5
allele num: 120464
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.189-4G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+977G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.148-4G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123-4G>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.131-4G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.148-4G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.28-4G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+977G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.148-4G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.182-4G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.148-4G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.242-4G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.148-4G>A
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.27-4G>A
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11060
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*123-4G>A
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

11-114311378-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311378
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311378
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 120552
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.182A>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.148A>T
  hgvsp: ENSP00000440665.1:p.Met50Leu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.148A>T
  hgvsp: ENSP00000443842.1:p.Met50Leu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.131A>T
  hgvsp: ENSP00000441639.1:p.Met45Leu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.27A>T
  hgvsp: ENSP00000441844.1:p.Met10Leu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.148A>T
  hgvsp: ENSP00000442703.1:p.Met50Leu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*123A>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+981A>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.28A>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.148A>T
  hgvsp: ENSP00000437460.1:p.Met50Leu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.148A>T
  hgvsp: ENSP00000265881.5:p.Met50Leu
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.189A>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.242A>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+981A>T
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10962
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met50Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

11-114311380-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311380
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311380
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 120578
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.133G>C
  hgvsp: ENSP00000441639.1:p.Met45Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.150G>C
  hgvsp: ENSP00000437460.1:p.Met50Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.29G>C
  hgvsp: ENSP00000441844.1:p.Met10Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.30G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.244G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.150G>C
  hgvsp: ENSP00000440665.1:p.Met50Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+983G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.150G>C
  hgvsp: ENSP00000265881.5:p.Met50Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.184G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.191G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.150G>C
  hgvsp: ENSP00000442703.1:p.Met50Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.150G>C
  hgvsp: ENSP00000443842.1:p.Met50Ile
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+983G>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*125G>C
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met50Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

11-114311382-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311382
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311383
    reference: chr 11
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+985_94+986insT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.152_153insT
  hgvsp: ENSP00000437460.1:p.Gly52ArgfsTer5
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*127_*128insT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.193_194insT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.152_153insT
  hgvsp: ENSP00000442703.1:p.Gly52ArgfsTer5
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.186_187insT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.135_136insT
  hgvsp: ENSP00000441639.1:p.Gly47ArgfsTer5
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.152_153insT
  hgvsp: ENSP00000265881.5:p.Gly52ArgfsTer5
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.152_153insT
  hgvsp: ENSP00000443842.1:p.Gly52ArgfsTer5
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+985_147+986insT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.32_33insT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.152_153insT
  hgvsp: ENSP00000440665.1:p.Gly52ArgfsTer5
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.31_32insT
  hgvsp: ENSP00000441844.1:p.Gly12ArgfsTer5
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.246_247insT
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11117
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly52ArgfsTer5
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

11-114311383-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311383
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311383
    reference: chr 11
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.153A>G
  hgvsp: ENST00000544196.1:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.194A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.32A>G
  hgvsp: ENST00000544827.1:c.32A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.153A>G
  hgvsp: ENST00000541703.1:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.153A>G
  hgvsp: ENST00000265881.5:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.136A>G
  hgvsp: ENST00000538198.1:c.136A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*128A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.153A>G
  hgvsp: ENST00000539275.1:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.33A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.153A>G
  hgvsp: ENST00000539754.1:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.247A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+986A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+986A>G
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.187A>G
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr51Thr
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

11-114311385-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311385
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311384
    reference: chr 11
allele count: 1
allele frequency: 8.286377195889957e-6
allele num: 120680
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*131delA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.156delA
  hgvsp: ENSP00000443842.1:p.Leu53TrpfsTer14
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+989delA
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.156delA
  hgvsp: ENSP00000437460.1:p.Leu53TrpfsTer14
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.35delA
  hgvsp: ENSP00000441844.1:p.Leu13TrpfsTer14
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.190delA
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.250delA
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+989delA
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.36delA
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.156delA
  hgvsp: ENSP00000440665.1:p.Leu53TrpfsTer14
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.156delA
  hgvsp: ENSP00000442703.1:p.Leu53TrpfsTer14
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.197delA
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.156delA
  hgvsp: ENSP00000265881.5:p.Leu53TrpfsTer14
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.139delA
  hgvsp: ENSP00000441639.1:p.Leu48TrpfsTer14
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu53TrpfsTer14
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: GA
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-114311387-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311387
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311387
    reference: chr 11
allele count: 1
allele frequency: 8.284043275842073e-6
allele num: 120714
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.157T>C
  hgvsp: ENST00000539275.1:c.157T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.157T>C
  hgvsp: ENST00000265881.5:c.157T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.157T>C
  hgvsp: ENST00000539754.1:c.157T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.36T>C
  hgvsp: ENST00000544827.1:c.36T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.157T>C
  hgvsp: ENST00000541703.1:c.157T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.37T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.198T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.157T>C
  hgvsp: ENST00000544196.1:c.157T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*132T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.191T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+990T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.251T>C
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.140T>C
  hgvsp: ENST00000538198.1:c.140T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+990T>C
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu53Leu
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

11-114311389-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311389
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311389
    reference: chr 11
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.159G>T
  hgvsp: ENSP00000265881.5:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+992G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.142G>T
  hgvsp: ENSP00000441639.1:p.Leu48Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.159G>T
  hgvsp: ENSP00000440665.1:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.159G>T
  hgvsp: ENSP00000437460.1:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*134G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.193G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.39G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.38G>T
  hgvsp: ENSP00000441844.1:p.Leu13Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.200G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.159G>T
  hgvsp: ENSP00000442703.1:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.159G>T
  hgvsp: ENSP00000443842.1:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+992G>T
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.253G>T
  variant of: http://identifiers.org/hgnc/17851
canonical: true
consequence: missense
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu53Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

11-114311389-GGACAT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114311389
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 114311384
    reference: chr 11
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437460
  ensembl transcript: ENST00000544196
  gene symbol: REXO2
  hgvsc: ENST00000544196.1:c.160_164delGACAT
  hgvsp: ENSP00000437460.1:p.Asp54Ter
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000539333
  gene symbol: REXO2
  hgvsc: ENST00000539333.1:n.201_205delGACAT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442703
  ensembl transcript: ENST00000541703
  gene symbol: REXO2
  hgvsc: ENST00000541703.1:c.160_164delGACAT
  hgvsp: ENSP00000442703.1:p.Asp54Ter
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441639
  ensembl transcript: ENST00000538198
  gene symbol: REXO2
  hgvsc: ENST00000538198.1:c.143_147delGACAT
  hgvsp: ENSP00000441639.1:p.Asp49Ter
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000543243
  gene symbol: REXO2
  hgvsc: ENST00000543243.1:n.194_198delGACAT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000437380
  ensembl transcript: ENST00000546316
  gene symbol: REXO2
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000441844
  ensembl transcript: ENST00000544827
  gene symbol: REXO2
  hgvsc: ENST00000544827.1:c.39_43delGACAT
  hgvsp: ENSP00000441844.1:p.Asp14Ter
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000440665
  ensembl transcript: ENST00000539754
  gene symbol: REXO2
  hgvsc: ENST00000539754.1:c.160_164delGACAT
  hgvsp: ENSP00000440665.1:p.Asp54Ter
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000544010
  gene symbol: REXO2
  hgvsc: ENST00000544010.1:n.254_258delGACAT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000444421
  ensembl transcript: ENST00000539119
  gene symbol: REXO2
  hgvsc: ENST00000539119.1:c.94+993_94+997delGACAT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000443842
  ensembl transcript: ENST00000539275
  gene symbol: REXO2
  hgvsc: ENST00000539275.1:c.160_164delGACAT
  hgvsp: ENSP00000443842.1:p.Asp54Ter
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000265881
  ensembl transcript: ENST00000265881
  gene symbol: REXO2
  hgvsc: ENST00000265881.5:c.160_164delGACAT
  hgvsp: ENSP00000265881.5:p.Asp54Ter
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076043
  ensembl protein: ENSP00000442380
  ensembl transcript: ENST00000543131
  gene symbol: REXO2
  hgvsc: ENST00000543131.1:c.147+993_147+997delGACAT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076043
  ensembl transcript: ENST00000542186
  gene symbol: REXO2
  hgvsc: ENST00000542186.1:n.40_44delGACAT
  variant of: http://identifiers.org/hgnc/17851
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000255663
  ensembl protein: ENSP00000461728
  ensembl transcript: ENST00000544347
  gene symbol: RP11-212D19.4
  hgvsc: ENST00000544347.1:c.*135_*139delGACAT
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp54Ter
num of homozygotes: 0
population: African
population: Other
reference allele: GGACAT

GenotypeQuality
all individuals: 404
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4205
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1767
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2941
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33379
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.506584096090374e-5
allele num: 58778
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7932
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8104
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15226
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.94e-1

FS
type: SiteQuality
SIO_000300: 8.263e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.89e-1

QD
type: SiteQuality
SIO_000300: 1.305e1

DP
type: SiteQuality
SIO_000300: 1.313547e6

GenotypeQuality
all individuals: 771
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1767
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6378
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2941
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33379
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.701316819218075e-5
allele num: 58778
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7932
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15226
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-1

QD
type: SiteQuality
SIO_000300: 1.305e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

FS
type: SiteQuality
SIO_000300: 8.263e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.89e-1

DP
type: SiteQuality
SIO_000300: 1.313547e6

VQSLOD
type: SiteQuality
SIO_000300: 3.76e-1

GenotypeQuality
all individuals: 4192
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 184
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1805
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5990
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 100
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1206
bin: 9.75e1
variant carriers: 63

GenotypeQuality
all individuals: 638
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1731
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 62
allele frequency: 1.053024898943578e-3
allele num: 58878
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.232741617357002e-4
allele num: 8112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7964
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

FS
type: SiteQuality
SIO_000300: 3.116e0

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.118e1

DP
type: SiteQuality
SIO_000300: 1.331046e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.532e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.72e-1

GenotypeQuality
all individuals: 469
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1842
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1729
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 744
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34745
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4193
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6012
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 63
allele frequency: 1.068231144872491e-3
allele num: 58976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7980
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 3.690944881889764e-4
allele num: 8128
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.181e0

FS
type: SiteQuality
SIO_000300: 1.267e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.205e1

DP
type: SiteQuality
SIO_000300: 1.335526e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

GenotypeQuality
all individuals: 4252
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 9.75e1
variant carriers: 5

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8160
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.252191334835963e-4
allele num: 7986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.072022722661798e-5
allele num: 59148
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.531678641410843e-5
allele num: 15310
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-1

FS
type: SiteQuality
SIO_000300: 4.312e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

QD
type: SiteQuality
SIO_000300: 1.13e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.356e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.07e-1

DP
type: SiteQuality
SIO_000300: 1.340264e6

GenotypeQuality
all individuals: 163
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4252
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.453371204436329e-5
allele num: 59148
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7986
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.450980392156863e-4
allele num: 8160
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15310
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.312e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.356e0

QD
type: SiteQuality
SIO_000300: 1.13e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.340264e6

GenotypeQuality
all individuals: 503
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variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1576
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GenotypeQuality
all individuals: 323
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8204
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15362
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59332
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.545628102329134e-5
allele num: 10476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8010
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.877e0

VQSLOD
type: SiteQuality
SIO_000300: 6.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-2

QD
type: SiteQuality
SIO_000300: 1.144e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.348457e6

GenotypeQuality
all individuals: 99
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
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variant carriers: 0

GenotypeQuality
all individuals: 141
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 787
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variant carriers: 0

GenotypeQuality
all individuals: 110
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.439979392065946e-5
allele num: 15528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59832
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-1

DP
type: SiteQuality
SIO_000300: 1.376293e6

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.041e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.9e-3

GenotypeQuality
all individuals: 472
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5856
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variant carriers: 0

GenotypeQuality
all individuals: 118
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8370
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.668001067520683e-4
allele num: 59952
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8116
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4574
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.709e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.15e0

FS
type: SiteQuality
SIO_000300: 2.831e0

QD
type: SiteQuality
SIO_000300: 1.174e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.380222e6

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10602
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.31578947368421e-3
allele num: 760
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.664391997603276e-5
allele num: 60082
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.4538e1

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

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

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.383859e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.464e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.05e-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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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4702
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.288500835965076e-5
allele num: 10766
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60974
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15734
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.78e0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4716
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
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

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: 1
allele frequency: 9.266123054114158e-5
allele num: 10792
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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BaseQRankSum
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MQ
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.026e0

DP
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SIO_000300: 1.428064e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.636714786081377e-5
allele num: 61098
num of homozygotes: 0

QD
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VQSLOD
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DP
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MQ
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FS
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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SIO_000300: 2.43e-1

ClippingRankSum
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InbreedingCoeff
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SIO_000300: -2.6e-3

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 1.899455489426364e-4
allele num: 15794
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European (Non-Finnish)
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allele frequency: 0.0e0
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QD
type: SiteQuality
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.834e1

ClippingRankSum
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SIO_000300: -3.78e-1

DP
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SIO_000300: 1.435654e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10882
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.620115352213077e-5
allele num: 61724
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.867e1

MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.9e-3

ReadPosRankSum
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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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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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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15820
num of homozygotes: 0

Other
type: Population
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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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10878
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.617861187510112e-5
allele num: 61810
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8918
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4766
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 1.117568171658471e-4
allele num: 8948
num of homozygotes: 0

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

South Asian
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Other
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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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ClippingRankSum
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FS
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QD
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MQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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allele frequency: 5.28680941052075e-4
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European (Non-Finnish)
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allele frequency: 9.874592673052236e-5
allele num: 60762
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Latino
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East Asian
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DP
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
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South Asian
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East Asian
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Other
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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MQRankSum
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FS
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QD
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DP
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

MQ
type: SiteQuality
SIO_000300: 5.855e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

GenotypeDepth
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variant carriers: 21

GenotypeDepth
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variant carriers: 22

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 30

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 295

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 5

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 7.75e1
variant carriers: 3

GenotypeQuality
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bin: 5.25e1
variant carriers: 3

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 4429
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 263
bin: 8.25e1
variant carriers: 3

South Asian
type: Population
allele count: 1
allele frequency: 6.768647624204685e-5
allele num: 14774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.336447350860804e-5
allele num: 59944
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 1.459427904261529e-3
allele num: 10278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4360
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7940
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.351351351351351e-3
allele num: 740
num of homozygotes: 0

African
type: Population
allele count: 290
allele frequency: 3.312014618547282e-2
allele num: 8756
num of homozygotes: 2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

DP
type: SiteQuality
SIO_000300: 1.386966e6

BaseQRankSum
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SIO_000300: 2.17e0

VQSLOD
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SIO_000300: 4.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

FS
type: SiteQuality
SIO_000300: 1.143e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

QD
type: SiteQuality
SIO_000300: 1.202e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e-1

GenotypeDepth
all individuals: 21
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1045
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GenotypeQuality
all individuals: 37915
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8756
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7940
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.668223675430402e-5
allele num: 59944
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4360
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

FS
type: SiteQuality
SIO_000300: 1.143e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

QD
type: SiteQuality
SIO_000300: 1.202e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.386966e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e-1

GenotypeDepth
all individuals: 23
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variant carriers: 0

GenotypeDepth
all individuals: 628
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variant carriers: 0

GenotypeDepth
all individuals: 18
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 427
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variant carriers: 0

GenotypeQuality
all individuals: 92
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GenotypeQuality
all individuals: 678
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

GenotypeQuality
all individuals: 839
bin: 7.25e1
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GenotypeQuality
all individuals: 653
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4294
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.034401745259272e-5
allele num: 59590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7896
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.286e0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

ReadPosRankSum
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SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 1.373345e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

FS
type: SiteQuality
SIO_000300: 6.56e-1

QD
type: SiteQuality
SIO_000300: 1.322e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

GenotypeDepth
all individuals: 23
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
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variant carriers: 0

GenotypeDepth
all individuals: 628
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 1600
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 23026
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GenotypeQuality
all individuals: 217
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.87863986473793e-5
allele num: 53230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6974
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.187201e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

FS
type: SiteQuality
SIO_000300: 2.868e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.849e0

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

VQSLOD
type: SiteQuality
SIO_000300: -1.623e0

QD
type: SiteQuality
SIO_000300: 3.063e1

GenotypeDepth
all individuals: 2272
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
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variant carriers: 0

GenotypeDepth
all individuals: 13047
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2132
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1607
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 19239
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variant carriers: 0

GenotypeQuality
all individuals: 853
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 582
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GenotypeQuality
all individuals: 564
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12392
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.289324394017535e-4
allele num: 7756
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53254
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.187e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.185094e6

VQSLOD
type: SiteQuality
SIO_000300: -2.858e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

FS
type: SiteQuality
SIO_000300: 2.363e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

QD
type: SiteQuality
SIO_000300: 2.909e1

GenotypeDepth
all individuals: 14496
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 27
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GenotypeDepth
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GenotypeQuality
all individuals: 628
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 20597
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GenotypeQuality
all individuals: 2506
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GenotypeQuality
all individuals: 1945
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1105
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variant carriers: 5

GenotypeQuality
all individuals: 65
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.352082206598161e-4
allele num: 7396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.963266279716944e-5
allele num: 50308
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.184e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

DP
type: SiteQuality
SIO_000300: 1.11038e6

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

QD
type: SiteQuality
SIO_000300: 1.09e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

GenotypeDepth
all individuals: 19
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variant carriers: 1

GenotypeDepth
all individuals: 19
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variant carriers: 1

GenotypeDepth
all individuals: 28
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GenotypeDepth
all individuals: 30
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GenotypeQuality
all individuals: 177
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 1423
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variant carriers: 341

GenotypeQuality
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GenotypeQuality
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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: 2190
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GenotypeQuality
all individuals: 64
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GenotypeQuality
all individuals: 476
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 11
allele frequency: 1.544509969109801e-3
allele num: 7122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 6.41025641025641e-4
allele num: 3120
num of homozygotes: 0

Latino
type: Population
allele count: 23
allele frequency: 3.2559456398641e-3
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Other
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European (Non-Finnish)
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allele frequency: 6.548391146073057e-3
allele num: 47798
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South Asian
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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MQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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FS
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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Other
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East Asian
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South Asian
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Latino
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African
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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DP
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QD
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ClippingRankSum
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BaseQRankSum
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FS
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

Latino
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num of homozygotes: 0

African
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allele frequency: 1.865091700341933e-3
allele num: 6434
num of homozygotes: 0

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

European (Finnish)
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South Asian
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Latino
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Other
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European (Non-Finnish)
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East Asian
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MQ
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BaseQRankSum
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ClippingRankSum
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DP
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VQSLOD
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MQRankSum
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QD
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InbreedingCoeff
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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FS
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InbreedingCoeff
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MQ
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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MQRankSum
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VQSLOD
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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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Latino
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African
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South Asian
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East Asian
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European (Non-Finnish)
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European (Finnish)
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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VQSLOD
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 88

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 10965
bin: 7.5e0
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GenotypeQuality
all individuals: 759
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 3.054367745876604e-4
allele num: 3274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4882
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 3.029336734693877e-3
allele num: 6272
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 54
allele frequency: 1.879568395405499e-3
allele num: 28730
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 1.744186046511628e-2
allele num: 344
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.25e-2

QD
type: SiteQuality
SIO_000300: 1.296e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.96168e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 452
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variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 1361
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 488
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GenotypeQuality
all individuals: 1806
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25990
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1446
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2796
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4570
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.32e-1

DP
type: SiteQuality
SIO_000300: 6.58613e5

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

MQRankSum
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SIO_000300: -3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -1.221e0

QD
type: SiteQuality
SIO_000300: 1.152e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.76e-2

GenotypeDepth
all individuals: 23
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variant carriers: 0

GenotypeDepth
all individuals: 13
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variant carriers: 0

GenotypeDepth
all individuals: 31
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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
all individuals: 1095
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variant carriers: 8

GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 353
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2638
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.615062761506276e-4
allele num: 3824
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 998
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4028
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.960015680125441e-4
allele num: 20408
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1824
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.79719e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.81e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

FS
type: SiteQuality
SIO_000300: 6.69e-1

QD
type: SiteQuality
SIO_000300: 1.244e1

VQSLOD
type: SiteQuality
SIO_000300: 2.97e0

GenotypeDepth
all individuals: 22
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variant carriers: 0

GenotypeDepth
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 23928
bin: 7.5e0
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GenotypeQuality
all individuals: 22684
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 337
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variant carriers: 0

GenotypeQuality
all individuals: 1278
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GenotypeQuality
all individuals: 1088
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 123
bin: 7.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1506
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 129
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GenotypeQuality
all individuals: 53
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GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 262
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17020
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 6.422607578676942e-4
allele num: 3114
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3414
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.218e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 5.39119e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.876e0

QD
type: SiteQuality
SIO_000300: 7.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

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

GenotypeDepth
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 2332
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variant carriers: 0

GenotypeQuality
all individuals: 1631
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 24913
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 826
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 75
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GenotypeQuality
all individuals: 52
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GenotypeQuality
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GenotypeQuality
all individuals: 121
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GenotypeQuality
all individuals: 129
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variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2106
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 5.27474e5

QD
type: SiteQuality
SIO_000300: 7.35e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.81e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.628e0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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GenotypeQuality
all individuals: 64
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1993
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 75
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1230
bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 1085
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 66
bin: 4.25e1
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GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2944
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2064
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1696
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
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SIO_000300: -5.44e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 9.56e0

DP
type: SiteQuality
SIO_000300: 4.87712e5

VQSLOD
type: SiteQuality
SIO_000300: -9.343e-1

GenotypeDepth
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bin: 5.75e1
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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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2432
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1020
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VQSLOD
type: SiteQuality
SIO_000300: -1.932e0

ReadPosRankSum
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QD
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MQRankSum
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FS
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MQ
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ClippingRankSum
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SIO_000300: 7.31e-1

BaseQRankSum
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SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 4.28163e5

InbreedingCoeff
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SIO_000300: -6.279999999999999e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
all individuals: 4121
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 2376
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 970
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 462
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8290
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1034
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.25354e5

InbreedingCoeff
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SIO_000300: -6.45e-2

ClippingRankSum
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VQSLOD
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SIO_000300: -1.869e0

MQ
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SIO_000300: 6.0e1

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: -3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

QD
type: SiteQuality
SIO_000300: 9.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

GenotypeDepth
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bin: 7.5e0
variant carriers: 6

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

Other
type: Population
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: 850
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.327316166710911e-4
allele num: 7534
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 936
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2252
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
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SIO_000300: 4.08923e5

MQRankSum
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SIO_000300: 1.98e-1

QD
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FS
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BaseQRankSum
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SIO_000300: -1.307e0

ReadPosRankSum
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SIO_000300: 2.62e-1

ClippingRankSum
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SIO_000300: 1.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.660000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6974
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 86
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

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

DP
type: SiteQuality
SIO_000300: 3.96876e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: -1.708e-1

QD
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SIO_000300: 2.093e1

InbreedingCoeff
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SIO_000300: -6.850000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2000
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 80
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.047e1

InbreedingCoeff
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SIO_000300: -7.149999999999999e-2

MQRankSum
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SIO_000300: -1.38e0

ClippingRankSum
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DP
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SIO_000300: 3.9188e5

MQ
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SIO_000300: 5.682e1

VQSLOD
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SIO_000300: -1.284e0

ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 132
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variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.383125864453665e-4
allele num: 7230
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

African
type: Population
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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2494
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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MQRankSum
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QD
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FS
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ClippingRankSum
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SIO_000300: 5.93e-1

BaseQRankSum
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ReadPosRankSum
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SIO_000300: 1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.36e-2

DP
type: SiteQuality
SIO_000300: 1.25341e5

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 2
allele frequency: 2.76625172890733e-4
allele num: 7230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2494
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

QD
type: SiteQuality
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BaseQRankSum
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VQSLOD
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MQRankSum
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FS
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ReadPosRankSum
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MQ
type: SiteQuality
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ClippingRankSum
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SIO_000300: 5.93e-1

DP
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2500
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Latino
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Other
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South Asian
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allele num: 7238
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BaseQRankSum
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VQSLOD
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FS
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QD
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ClippingRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 3

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

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

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

GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66238
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (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: 0.0e0
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num of homozygotes: 0

MQ
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FS
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VQSLOD
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InbreedingCoeff
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DP
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QD
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GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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VQSLOD
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DP
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QD
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FS
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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num of homozygotes: 0

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

Other
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South Asian
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Latino
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num of homozygotes: 0

African
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FS
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QD
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQ
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SIO_000300: 5.365e1

GenotypeDepth
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variant carriers: 0

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

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 66316
num of homozygotes: 0

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

East Asian
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Other
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African
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num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.29e0

FS
type: SiteQuality
SIO_000300: 9.513e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 6.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

DP
type: SiteQuality
SIO_000300: 2.265607e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeDepth
all individuals: 10598
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6403
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3980
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 555
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1138
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 703
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4265
bin: 8.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 3675
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20572
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5608
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16425
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2862
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4437
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

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