http://identifiers.org/exac.variant/11-72012799-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012799
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012800
    reference: chr 11
allele count: 1
allele frequency: 8.542481761801439e-6
allele num: 117062
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.816+47_816+48insT
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1434+47_1434+48insT
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.752+47_752+48insT
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1329+47_1329+48insT
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1242+47_1242+48insT
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1329+47_1329+48insT
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.243+47_243+48insT
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1419+47_1419+48insT
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1284+47_1284+48insT
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3497
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1720
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1959
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3764
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

11-72012800-T-TATCTCCAGGTGTCCCCCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012800
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012818
    reference: chr 11
allele count: 1
allele frequency: 8.537085097664253e-6
allele num: 117136
alternate allele: TATCTCCAGGTGTCCCCCC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1763
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3519
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29310
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

11-72012801-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012801
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012801
    reference: chr 11
allele count: 1
allele frequency: 8.538105565137207e-6
allele num: 117122
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.816+46A>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1434+46A>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1329+46A>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1329+46A>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.243+46A>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1284+46A>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.752+46A>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1242+46A>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1419+46A>C
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2156
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

11-72012806-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012806
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012806
    reference: chr 11
allele count: 1
allele frequency: 8.532277606184194e-6
allele num: 117202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1284+41G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.816+41G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1242+41G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.752+41G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1329+41G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1329+41G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.243+41G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1434+41G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1419+41G>A
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5853
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3526
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29310
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

11-72012813-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012813
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012814
    reference: chr 11
allele count: 1
allele frequency: 8.519774396373984e-6
allele num: 117374
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1284+33dupG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.243+33dupG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.816+33dupG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1434+33dupG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1329+33dupG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1329+33dupG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.752+33dupG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1419+33dupG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1242+33dupG
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3530
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

11-72012814-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012814
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012814
    reference: chr 11
allele count: 1
allele frequency: 8.516581784734879e-6
allele num: 117418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.243+33G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1329+33G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.752+33G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1434+33G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1284+33G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1419+33G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1329+33G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.816+33G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1242+33G>A
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3716
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3561
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-72012815-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012815
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012815
    reference: chr 11
allele count: 1
allele frequency: 8.510493438409559e-6
allele num: 117502
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1284+32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1419+32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1434+32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1329+32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.752+32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1329+32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.243+32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.816+32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1242+32G>A
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1975
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3576
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7317
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-72012819-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012819
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012819
    reference: chr 11
allele count: 1
allele frequency: 8.487955591016347e-6
allele num: 117814
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1284+28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1419+28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.243+28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1434+28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.816+28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.752+28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1329+28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1329+28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1242+28G>T
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3771
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3539
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7766
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-72012819-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012819
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012819
    reference: chr 11
allele count: 2
allele frequency: 1.697591118203269e-5
allele num: 117814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.816+28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1434+28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1329+28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.243+28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.752+28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1329+28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1284+28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1242+28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1419+28G>C
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3727
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7766
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1985
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

11-72012819-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012819
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012819
    reference: chr 11
allele count: 5
allele frequency: 4.243977795508174e-5
allele num: 117814
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1419+28G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1242+28G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.752+28G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1329+28G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.816+28G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1329+28G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.243+28G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1434+28G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1284+28G>A
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8256
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29309
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1835
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

11-72012820-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012820
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012820
    reference: chr 11
allele count: 1
allele frequency: 8.47443263673497e-6
allele num: 118002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1329+27C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1242+27C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1329+27C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1419+27C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.243+27C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.752+27C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1284+27C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.816+27C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1434+27C>T
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3547
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8104
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3772
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-72012834-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012834
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012834
    reference: chr 11
allele count: 3
allele frequency: 2.517581108071365e-5
allele num: 119162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.816+13G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.243+13G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1284+13G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1329+13G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1434+13G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1329+13G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.752+13G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1419+13G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1242+13G>T
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2159
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29304
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3731
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD

11-72012840-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012840
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012840
    reference: chr 11
allele count: 1
allele frequency: 8.357151214294072e-6
allele num: 119658
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1284+7C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.816+7C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.243+7C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1329+7C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.752+7C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1329+7C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1419+7C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1242+7C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1434+7C>G
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8263
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 3.25e1
  variant carriers: 0
hgvs: c.1419+7C>G
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

11-72012856-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012856
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012856
    reference: chr 11
allele count: 1
allele frequency: 8.288987251537607e-6
allele num: 120642
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.807G>C
  hgvsp: ENST00000543042.1:c.807G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1320G>C
  hgvsp: ENST00000535477.1:c.1320G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1425G>C
  hgvsp: ENST00000535990.1:c.1425G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1275G>C
  hgvsp: ENST00000437826.2:c.1275G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1233G>C
  hgvsp: ENST00000340729.5:c.1233G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.743G>C
  hgvsp: ENST00000544382.1:c.743G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1320G>C
  hgvsp: ENST00000538039.1:c.1320G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.234G>C
  hgvsp: ENST00000538021.1:c.234G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1410G>C
  hgvsp: ENST00000294053.3:c.1410G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8046
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu470Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

11-72012856-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012856
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012856
    reference: chr 11
allele count: 1
allele frequency: 8.288987251537607e-6
allele num: 120642
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.743G>A
  hgvsp: ENST00000544382.1:c.743G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1425G>A
  hgvsp: ENST00000535990.1:c.1425G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1410G>A
  hgvsp: ENST00000294053.3:c.1410G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.807G>A
  hgvsp: ENST00000543042.1:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1275G>A
  hgvsp: ENST00000437826.2:c.1275G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1320G>A
  hgvsp: ENST00000535477.1:c.1320G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1233G>A
  hgvsp: ENST00000340729.5:c.1233G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.234G>A
  hgvsp: ENST00000538021.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1320G>A
  hgvsp: ENST00000538039.1:c.1320G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu470Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

11-72012876-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012876
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012876
    reference: chr 11
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1255C>T
  hgvsp: ENSP00000407296.2:p.Leu419Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1405C>T
  hgvsp: ENSP00000443822.1:p.Leu469Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.214C>T
  hgvsp: ENSP00000445180.1:p.Leu72Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.787C>T
  hgvsp: ENSP00000439746.1:p.Leu263Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1390C>T
  hgvsp: ENSP00000294053.3:p.Leu464Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1300C>T
  hgvsp: ENSP00000441518.1:p.Leu434Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1300C>T
  hgvsp: ENSP00000440423.1:p.Leu434Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.723C>T
  hgvsp: ENSP00000438372.1:p.Leu242Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1213C>T
  hgvsp: ENSP00000340385.5:p.Leu405Phe
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3892
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu464Phe
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

11-72012882-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012882
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012883
    reference: chr 11
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1293dupA
  hgvsp: ENSP00000441518.1:p.Asp432ArgfsTer11
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1383dupA
  hgvsp: ENSP00000294053.3:p.Asp462ArgfsTer11
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1398dupA
  hgvsp: ENSP00000443822.1:p.Asp467ArgfsTer11
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.716dupA
  hgvsp: ENSP00000438372.1:p.Asp240ArgfsTer11
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.780dupA
  hgvsp: ENSP00000439746.1:p.Asp261ArgfsTer11
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.207dupA
  hgvsp: ENSP00000445180.1:p.Asp70ArgfsTer11
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1293dupA
  hgvsp: ENSP00000440423.1:p.Asp432ArgfsTer11
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1248dupA
  hgvsp: ENSP00000407296.2:p.Asp417ArgfsTer11
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1206dupA
  hgvsp: ENSP00000340385.5:p.Asp403ArgfsTer11
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp462ArgfsTer11
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum

11-72012883-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012883
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012883
    reference: chr 11
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1206A>G
  hgvsp: ENST00000340729.5:c.1206A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1398A>G
  hgvsp: ENST00000535990.1:c.1398A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.716A>G
  hgvsp: ENST00000544382.1:c.716A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1383A>G
  hgvsp: ENST00000294053.3:c.1383A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1248A>G
  hgvsp: ENST00000437826.2:c.1248A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.207A>G
  hgvsp: ENST00000538021.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.780A>G
  hgvsp: ENST00000543042.1:c.780A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1293A>G
  hgvsp: ENST00000535477.1:c.1293A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1293A>G
  hgvsp: ENST00000538039.1:c.1293A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3589
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2059
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro461Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

11-72012884-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012884
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012884
    reference: chr 11
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.715C>T
  hgvsp: ENSP00000438372.1:p.Pro239Leu
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1292C>T
  hgvsp: ENSP00000440423.1:p.Pro431Leu
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.779C>T
  hgvsp: ENSP00000439746.1:p.Pro260Leu
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1397C>T
  hgvsp: ENSP00000443822.1:p.Pro466Leu
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.206C>T
  hgvsp: ENSP00000445180.1:p.Pro69Leu
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1382C>T
  hgvsp: ENSP00000294053.3:p.Pro461Leu
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1247C>T
  hgvsp: ENSP00000407296.2:p.Pro416Leu
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1205C>T
  hgvsp: ENSP00000340385.5:p.Pro402Leu
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1292C>T
  hgvsp: ENSP00000441518.1:p.Pro431Leu
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2060
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro461Leu
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

11-72012887-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012887
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012887
    reference: chr 11
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.203A>G
  hgvsp: ENSP00000445180.1:p.His68Arg
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1394A>G
  hgvsp: ENSP00000443822.1:p.His465Arg
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1202A>G
  hgvsp: ENSP00000340385.5:p.His401Arg
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1289A>G
  hgvsp: ENSP00000441518.1:p.His430Arg
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.776A>G
  hgvsp: ENSP00000439746.1:p.His259Arg
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.712A>G
  hgvsp: ENSP00000438372.1:p.His238Arg
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1244A>G
  hgvsp: ENSP00000407296.2:p.His415Arg
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1289A>G
  hgvsp: ENSP00000440423.1:p.His430Arg
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1379A>G
  hgvsp: ENSP00000294053.3:p.His460Arg
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His460Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

11-72012889-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012889
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012889
    reference: chr 11
allele count: 28
allele frequency: 2.308440648342045e-4
allele num: 121294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1200C>T
  hgvsp: ENST00000340729.5:c.1200C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.774C>T
  hgvsp: ENST00000543042.1:c.774C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1242C>T
  hgvsp: ENST00000437826.2:c.1242C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1377C>T
  hgvsp: ENST00000294053.3:c.1377C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1287C>T
  hgvsp: ENST00000535477.1:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1392C>T
  hgvsp: ENST00000535990.1:c.1392C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1287C>T
  hgvsp: ENST00000538039.1:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.710C>T
  hgvsp: ENST00000544382.1:c.710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.201C>T
  hgvsp: ENST00000538021.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12033
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2056
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala459Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

11-72012901-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012901
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012901
    reference: chr 11
allele count: 4
allele frequency: 3.296848213108268e-5
allele num: 121328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1275A>G
  hgvsp: ENST00000535477.1:c.1275A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.762A>G
  hgvsp: ENST00000543042.1:c.762A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1365A>G
  hgvsp: ENST00000294053.3:c.1365A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.698A>G
  hgvsp: ENST00000544382.1:c.698A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1188A>G
  hgvsp: ENST00000340729.5:c.1188A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.189A>G
  hgvsp: ENST00000538021.1:c.189A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1230A>G
  hgvsp: ENST00000437826.2:c.1230A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1380A>G
  hgvsp: ENST00000535990.1:c.1380A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1275A>G
  hgvsp: ENST00000538039.1:c.1275A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6790
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu455Glu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

11-72012920-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012920
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012920
    reference: chr 11
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.170C>T
  hgvsp: ENSP00000445180.1:p.Ala57Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1256C>T
  hgvsp: ENSP00000441518.1:p.Ala419Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1346C>T
  hgvsp: ENSP00000294053.3:p.Ala449Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1256C>T
  hgvsp: ENSP00000440423.1:p.Ala419Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.679C>T
  hgvsp: ENSP00000438372.1:p.Ala227Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.743C>T
  hgvsp: ENSP00000439746.1:p.Ala248Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1211C>T
  hgvsp: ENSP00000407296.2:p.Ala404Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1361C>T
  hgvsp: ENSP00000443822.1:p.Ala454Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1169C>T
  hgvsp: ENSP00000340385.5:p.Ala390Val
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6790
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala449Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

11-72012923-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012923
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012923
    reference: chr 11
allele count: 48
allele frequency: 3.954848809425723e-4
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1253A>G
  hgvsp: ENSP00000440423.1:p.Asn418Ser
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1358A>G
  hgvsp: ENSP00000443822.1:p.Asn453Ser
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.740A>G
  hgvsp: ENSP00000439746.1:p.Asn247Ser
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1343A>G
  hgvsp: ENSP00000294053.3:p.Asn448Ser
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1208A>G
  hgvsp: ENSP00000407296.2:p.Asn403Ser
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1166A>G
  hgvsp: ENSP00000340385.5:p.Asn389Ser
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.676A>G
  hgvsp: ENSP00000438372.1:p.Asn226Ser
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1253A>G
  hgvsp: ENSP00000441518.1:p.Asn418Ser
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.167A>G
  hgvsp: ENSP00000445180.1:p.Asn56Ser
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 9.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6792
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3590
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn448Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/11-72012929-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012929
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012929
    reference: chr 11
allele count: 5
allele frequency: 4.119566292060772e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1247G>T
  hgvsp: ENSP00000441518.1:p.Cys416Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1247G>T
  hgvsp: ENSP00000440423.1:p.Cys416Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1160G>T
  hgvsp: ENSP00000340385.5:p.Cys387Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.161G>T
  hgvsp: ENSP00000445180.1:p.Cys54Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.734G>T
  hgvsp: ENSP00000439746.1:p.Cys245Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1352G>T
  hgvsp: ENSP00000443822.1:p.Cys451Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.670G>T
  hgvsp: ENSP00000438372.1:p.Cys224Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1337G>T
  hgvsp: ENSP00000294053.3:p.Cys446Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1202G>T
  hgvsp: ENSP00000407296.2:p.Cys401Phe
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Cys446Phe
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: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-72012946-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012946
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012946
    reference: chr 11
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1335C>T
  hgvsp: ENST00000535990.1:c.1335C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.653C>T
  hgvsp: ENST00000544382.1:c.653C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.144C>T
  hgvsp: ENST00000538021.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1230C>T
  hgvsp: ENST00000535477.1:c.1230C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1230C>T
  hgvsp: ENST00000538039.1:c.1230C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.717C>T
  hgvsp: ENST00000543042.1:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1320C>T
  hgvsp: ENST00000294053.3:c.1320C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1185C>T
  hgvsp: ENST00000437826.2:c.1185C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1143C>T
  hgvsp: ENST00000340729.5:c.1143C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3909
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr440Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

11-72012946-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012946
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012946
    reference: chr 11
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1230C>A
  hgvsp: ENST00000538039.1:c.1230C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.144C>A
  hgvsp: ENST00000538021.1:c.144C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1185C>A
  hgvsp: ENST00000437826.2:c.1185C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.653C>A
  hgvsp: ENST00000544382.1:c.653C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1230C>A
  hgvsp: ENST00000535477.1:c.1230C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.717C>A
  hgvsp: ENST00000543042.1:c.717C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1320C>A
  hgvsp: ENST00000294053.3:c.1320C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1143C>A
  hgvsp: ENST00000340729.5:c.1143C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1335C>A
  hgvsp: ENST00000535990.1:c.1335C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr440Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

11-72012958-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012958
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012958
    reference: chr 11
allele count: 46
allele frequency: 3.790688092295014e-4
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.641T>C
  hgvsp: ENST00000544382.1:c.641T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1131T>C
  hgvsp: ENST00000340729.5:c.1131T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.705T>C
  hgvsp: ENST00000543042.1:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1218T>C
  hgvsp: ENST00000535477.1:c.1218T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1218T>C
  hgvsp: ENST00000538039.1:c.1218T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.132T>C
  hgvsp: ENST00000538021.1:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1323T>C
  hgvsp: ENST00000535990.1:c.1323T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1308T>C
  hgvsp: ENST00000294053.3:c.1308T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1173T>C
  hgvsp: ENST00000437826.2:c.1173T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8266
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 9.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12063
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3904
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly436Gly
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

11-72012974-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012974
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012974
    reference: chr 11
allele count: 2
allele frequency: 1.649348507339601e-5
allele num: 121260
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.625T>C
  hgvsp: ENSP00000438372.1:p.Val209Ala
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.116T>C
  hgvsp: ENSP00000445180.1:p.Val39Ala
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1115T>C
  hgvsp: ENSP00000340385.5:p.Val372Ala
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.689T>C
  hgvsp: ENSP00000439746.1:p.Val230Ala
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1157T>C
  hgvsp: ENSP00000407296.2:p.Val386Ala
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1202T>C
  hgvsp: ENSP00000440423.1:p.Val401Ala
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1307T>C
  hgvsp: ENSP00000443822.1:p.Val436Ala
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1292T>C
  hgvsp: ENSP00000294053.3:p.Val431Ala
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1202T>C
  hgvsp: ENSP00000441518.1:p.Val401Ala
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3784
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val431Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-72012975-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012975
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012975
    reference: chr 11
allele count: 7
allele frequency: 5.773862549077831e-5
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.624G>A
  hgvsp: ENSP00000438372.1:p.Val209Ile
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1114G>A
  hgvsp: ENSP00000340385.5:p.Val372Ile
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1201G>A
  hgvsp: ENSP00000440423.1:p.Val401Ile
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.115G>A
  hgvsp: ENSP00000445180.1:p.Val39Ile
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.688G>A
  hgvsp: ENSP00000439746.1:p.Val230Ile
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1156G>A
  hgvsp: ENSP00000407296.2:p.Val386Ile
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1201G>A
  hgvsp: ENSP00000441518.1:p.Val401Ile
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1306G>A
  hgvsp: ENSP00000443822.1:p.Val436Ile
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1291G>A
  hgvsp: ENSP00000294053.3:p.Val431Ile
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val431Ile
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

11-72012976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012976
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012976
    reference: chr 11
allele count: 6
allele frequency: 4.949759936643073e-5
allele num: 121218
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1290C>T
  hgvsp: ENST00000294053.3:c.1290C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.114C>T
  hgvsp: ENST00000538021.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1155C>T
  hgvsp: ENST00000437826.2:c.1155C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.623C>T
  hgvsp: ENST00000544382.1:c.623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1200C>T
  hgvsp: ENST00000535477.1:c.1200C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.687C>T
  hgvsp: ENST00000543042.1:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1305C>T
  hgvsp: ENST00000535990.1:c.1305C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1113C>T
  hgvsp: ENST00000340729.5:c.1113C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1200C>T
  hgvsp: ENST00000538039.1:c.1200C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3785
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr430Tyr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

11-72012991-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012991
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012991
    reference: chr 11
allele count: 1
allele frequency: 8.266649031148734e-6
allele num: 120968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.672G>A
  hgvsp: ENST00000543042.1:c.672G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1275G>A
  hgvsp: ENST00000294053.3:c.1275G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.608G>A
  hgvsp: ENST00000544382.1:c.608G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1185G>A
  hgvsp: ENST00000535477.1:c.1185G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1290G>A
  hgvsp: ENST00000535990.1:c.1290G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1185G>A
  hgvsp: ENST00000538039.1:c.1185G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1140G>A
  hgvsp: ENST00000437826.2:c.1140G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1098G>A
  hgvsp: ENST00000340729.5:c.1098G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.99G>A
  hgvsp: ENST00000538021.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly425Gly
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

11-72012995-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72012995
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72012995
    reference: chr 11
allele count: 2
allele frequency: 1.65461555007694e-5
allele num: 120874
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.604T>C
  hgvsp: ENSP00000438372.1:p.Ile202Thr
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.95T>C
  hgvsp: ENSP00000445180.1:p.Ile32Thr
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1286T>C
  hgvsp: ENSP00000443822.1:p.Ile429Thr
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1271T>C
  hgvsp: ENSP00000294053.3:p.Ile424Thr
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1181T>C
  hgvsp: ENSP00000441518.1:p.Ile394Thr
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1136T>C
  hgvsp: ENSP00000407296.2:p.Ile379Thr
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1094T>C
  hgvsp: ENSP00000340385.5:p.Ile365Thr
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.668T>C
  hgvsp: ENSP00000439746.1:p.Ile223Thr
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1181T>C
  hgvsp: ENSP00000440423.1:p.Ile394Thr
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29254
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile424Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

11-72013014-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013014
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013014
    reference: chr 11
allele count: 1
allele frequency: 8.326810664979099e-6
allele num: 120094
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1258-6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.655-6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.82-6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1123-6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.591-6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1168-6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1273-6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1081-6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1168-6T>C
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29249
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3555
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1258-6T>C
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

11-72013018-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013018
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013018
    reference: chr 11
allele count: 1
allele frequency: 8.335278231587371e-6
allele num: 119972
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1123-10C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.655-10C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1273-10C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1168-10C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.591-10C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1081-10C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1168-10C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.82-10C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1258-10C>G
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29249
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3663
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1563
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

11-72013038-GGCCTTTCTGT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013038
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013028
    reference: chr 11
allele count: 2
allele frequency: 1.680700515975058e-5
allele num: 118998
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6798
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1964
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2363
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7009
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: GGCCTTTCTGT
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

11-72013040-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013040
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013040
    reference: chr 11
allele count: 1
allele frequency: 8.419209267865562e-6
allele num: 118776
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.82-32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1168-32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1273-32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.655-32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1081-32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1123-32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.591-32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1258-32G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1168-32G>A
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8200
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6796
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3777
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS

11-72013043-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013043
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013043
    reference: chr 11
allele count: 20
allele frequency: 1.686824216048446e-4
allele num: 118566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.655-35A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.591-35A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1273-35A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1258-35A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1168-35A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1168-35A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.82-35A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1123-35A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1081-35A>G
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7605
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6793
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3451
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29225
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 3499
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

11-72013297-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013297
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013297
    reference: chr 11
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.654+51A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.590+51A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1122+51A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1167+51A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1080+51A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.81+51A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1257+51A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.115T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1167+51A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1272+51A>G
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15357
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5141
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9987
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2395
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/11-72013318-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013318
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013318
    reference: chr 11
allele count: 1
allele frequency: 8.251914444151043e-6
allele num: 121184
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1167+30T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1272+30T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.654+30T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.81+30T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1122+30T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.590+30T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1167+30T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1080+30T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.136A>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1257+30T>G
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6943
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4916
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

11-72013319-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013319
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013319
    reference: chr 11
allele count: 1
allele frequency: 8.251778258214646e-6
allele num: 121186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.81+29A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1167+29A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1122+29A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.137T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1080+29A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1167+29A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.590+29A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.654+29A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1272+29A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1257+29A>G
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3621
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9197
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

11-72013323-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013323
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013322
    reference: chr 11
allele count: 6
allele frequency: 4.950495049504951e-5
allele num: 121200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1167+24delG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.142delC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1122+24delG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.654+24delG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.590+24delG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1272+24delG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1167+24delG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1080+24delG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.81+24delG
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1257+24delG
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3789
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9908
  bin: 9.75e1
  variant carriers: 6
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: TC
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

11-72013337-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013337
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013337
    reference: chr 11
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1257+11A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.155T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.81+11A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1167+11A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1080+11A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1122+11A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1272+11A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.654+11A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.590+11A>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1167+11A>G
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24793
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

11-72013342-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013342
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013342
    reference: chr 11
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.654+6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1167+6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1167+6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1272+6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.160A>G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1122+6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1257+6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1080+6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.81+6T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.590+6T>C
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1257+6T>C
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

11-72013345-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013345
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013345
    reference: chr 11
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1167+3G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.163C>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1272+3G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1167+3G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.654+3G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.81+3G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1080+3G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1122+3G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1257+3G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.590+3G>A
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
hgvs: c.1257+3G>A
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

11-72013351-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013351
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013351
    reference: chr 11
allele count: 23
allele frequency: 1.896656935991952e-4
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1164C>T
  hgvsp: ENST00000535477.1:c.1164C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1077C>T
  hgvsp: ENST00000340729.5:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1269C>T
  hgvsp: ENST00000535990.1:c.1269C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1254C>T
  hgvsp: ENST00000294053.3:c.1254C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.587C>T
  hgvsp: ENST00000544382.1:c.587C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1164C>T
  hgvsp: ENST00000538039.1:c.1164C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.78C>T
  hgvsp: ENST00000538021.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1119C>T
  hgvsp: ENST00000437826.2:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.169G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.651C>T
  hgvsp: ENST00000543042.1:c.651C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6496
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2346
  bin: 9.25e1
  variant carriers: 0
hgvs: p.His418His
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

11-72013351-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013351
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013351
    reference: chr 11
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1269C>G
  hgvsp: ENSP00000443822.1:p.His423Gln
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1077C>G
  hgvsp: ENSP00000340385.5:p.His359Gln
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1254C>G
  hgvsp: ENSP00000294053.3:p.His418Gln
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.587C>G
  hgvsp: ENSP00000438372.1:p.His196Gln
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1119C>G
  hgvsp: ENSP00000407296.2:p.His373Gln
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1164C>G
  hgvsp: ENSP00000440423.1:p.His388Gln
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.169G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.78C>G
  hgvsp: ENSP00000445180.1:p.His26Gln
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1164C>G
  hgvsp: ENSP00000441518.1:p.His388Gln
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.651C>G
  hgvsp: ENSP00000439746.1:p.His217Gln
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His418Gln
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS

11-72013356-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013356
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013356
    reference: chr 11
allele count: 4
allele frequency: 3.298098646130506e-5
allele num: 121282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.582C>T
  hgvsp: ENSP00000438372.1:p.Arg195Ter
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1072C>T
  hgvsp: ENSP00000340385.5:p.Arg358Ter
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.646C>T
  hgvsp: ENSP00000439746.1:p.Arg216Ter
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.73C>T
  hgvsp: ENSP00000445180.1:p.Arg25Ter
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1264C>T
  hgvsp: ENSP00000443822.1:p.Arg422Ter
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1114C>T
  hgvsp: ENSP00000407296.2:p.Arg372Ter
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1159C>T
  hgvsp: ENSP00000441518.1:p.Arg387Ter
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1159C>T
  hgvsp: ENSP00000440423.1:p.Arg387Ter
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1249C>T
  hgvsp: ENSP00000294053.3:p.Arg417Ter
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.174G>A
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6946
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg417Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

11-72013369-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013369
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013369
    reference: chr 11
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1251C>T
  hgvsp: ENST00000535990.1:c.1251C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1146C>T
  hgvsp: ENST00000538039.1:c.1146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1146C>T
  hgvsp: ENST00000535477.1:c.1146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1236C>T
  hgvsp: ENST00000294053.3:c.1236C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.60C>T
  hgvsp: ENST00000538021.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.633C>T
  hgvsp: ENST00000543042.1:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.569C>T
  hgvsp: ENST00000544382.1:c.569C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.187G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1059C>T
  hgvsp: ENST00000340729.5:c.1059C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1101C>T
  hgvsp: ENST00000437826.2:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15491
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser412Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

11-72013375-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013375
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013375
    reference: chr 11
allele count: 7
allele frequency: 5.77062586559388e-5
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.563C>T
  hgvsp: ENST00000544382.1:c.563C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.54C>T
  hgvsp: ENST00000538021.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.627C>T
  hgvsp: ENST00000543042.1:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1140C>T
  hgvsp: ENST00000535477.1:c.1140C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1053C>T
  hgvsp: ENST00000340729.5:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1245C>T
  hgvsp: ENST00000535990.1:c.1245C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.193G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1230C>T
  hgvsp: ENST00000294053.3:c.1230C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1095C>T
  hgvsp: ENST00000437826.2:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1140C>T
  hgvsp: ENST00000538039.1:c.1140C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp410Asp
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS

11-72013383-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013383
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013383
    reference: chr 11
allele count: 27
allele frequency: 2.225886232481451e-4
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1087A>T
  hgvsp: ENSP00000407296.2:p.Arg363Trp
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.555A>T
  hgvsp: ENSP00000438372.1:p.Arg186Trp
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1045A>T
  hgvsp: ENSP00000340385.5:p.Arg349Trp
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.46A>T
  hgvsp: ENSP00000445180.1:p.Arg16Trp
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.619A>T
  hgvsp: ENSP00000439746.1:p.Arg207Trp
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.201T>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1237A>T
  hgvsp: ENSP00000443822.1:p.Arg413Trp
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1132A>T
  hgvsp: ENSP00000440423.1:p.Arg378Trp
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1132A>T
  hgvsp: ENSP00000441518.1:p.Arg378Trp
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1222A>T
  hgvsp: ENSP00000294053.3:p.Arg408Trp
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4901
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg408Trp
num of homozygotes: 1
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-72013383-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013383
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013383
    reference: chr 11
allele count: 21
allele frequency: 1.731244847485573e-4
allele num: 121300
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1222A>G
  hgvsp: ENSP00000294053.3:p.Arg408Gly
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.619A>G
  hgvsp: ENSP00000439746.1:p.Arg207Gly
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.46A>G
  hgvsp: ENSP00000445180.1:p.Arg16Gly
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.201T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1045A>G
  hgvsp: ENSP00000340385.5:p.Arg349Gly
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1087A>G
  hgvsp: ENSP00000407296.2:p.Arg363Gly
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.555A>G
  hgvsp: ENSP00000438372.1:p.Arg186Gly
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1132A>G
  hgvsp: ENSP00000440423.1:p.Arg378Gly
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1132A>G
  hgvsp: ENSP00000441518.1:p.Arg378Gly
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1237A>G
  hgvsp: ENSP00000443822.1:p.Arg413Gly
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg408Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/11-72013391-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013391
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013391
    reference: chr 11
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1124G>T
  hgvsp: ENSP00000440423.1:p.Gly375Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1079G>T
  hgvsp: ENSP00000407296.2:p.Gly360Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1214G>T
  hgvsp: ENSP00000294053.3:p.Gly405Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.547G>T
  hgvsp: ENSP00000438372.1:p.Gly183Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1124G>T
  hgvsp: ENSP00000441518.1:p.Gly375Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.38G>T
  hgvsp: ENSP00000445180.1:p.Gly13Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1037G>T
  hgvsp: ENSP00000340385.5:p.Gly346Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.209C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.611G>T
  hgvsp: ENSP00000439746.1:p.Gly204Val
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1229G>T
  hgvsp: ENSP00000443822.1:p.Gly410Val
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly405Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-72013395-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013395
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013395
    reference: chr 11
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.546-3C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1123-3C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1228-3C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.213G>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1078-3C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.610-3C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1213-3C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.34C>A
  hgvsp: ENSP00000445180.1:p.Gln12Lys
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1036-3C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1123-3C>A
  variant of: http://identifiers.org/hgnc/30664
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15499
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln12Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

11-72013400-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013400
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013400
    reference: chr 11
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.610-8C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1123-8C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1123-8C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.29C>T
  hgvsp: ENSP00000445180.1:p.Ser10Phe
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1078-8C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.546-8C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.218G>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1036-8C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1213-8C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1228-8C>T
  variant of: http://identifiers.org/hgnc/30664
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser10Phe
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

11-72013406-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013406
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013406
    reference: chr 11
allele count: 2
allele frequency: 1.649049323065253e-5
allele num: 121282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.546-14T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.224A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1036-14T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1213-14T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.23T>C
  hgvsp: ENSP00000445180.1:p.Leu8Pro
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1123-14T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.610-14T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1228-14T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1123-14T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1078-14T>C
  variant of: http://identifiers.org/hgnc/30664
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu8Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

11-72013414-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013414
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013414
    reference: chr 11
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.546-22G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1036-22G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.15G>A
  hgvsp: ENSP00000445180.1:p.Trp5Ter
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.224+8C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1078-22G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1228-22G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1123-22G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.610-22G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1213-22G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1123-22G>A
  variant of: http://identifiers.org/hgnc/30664
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3606
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Trp5Ter
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/11-72013418-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013418
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013418
    reference: chr 11
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.12-1G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.610-26G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1123-26G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1036-26G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1213-26G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1123-26G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.224+12C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.546-26G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1078-26G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1228-26G>T
  variant of: http://identifiers.org/hgnc/30664
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2344
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.25e1
  variant carriers: 0
hgvs: c.12-1G>T
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/11-72013420-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013420
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013420
    reference: chr 11
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1123-28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.546-28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1078-28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1213-28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.224+14C>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.12-3G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.610-28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1228-28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1123-28G>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1036-28G>T
  variant of: http://identifiers.org/hgnc/30664
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4893
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: c.12-3G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD

11-72013420-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013420
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013420
    reference: chr 11
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.546-28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1123-28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.610-28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1036-28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.12-3G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1213-28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1123-28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1078-28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1228-28G>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.224+14C>G
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
hgvs: c.12-3G>C
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP

11-72013421-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013421
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013421
    reference: chr 11
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.224+15C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.610-29G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.12-4G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.546-29G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1123-29G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1123-29G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1213-29G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1228-29G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1078-29G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1036-29G>A
  variant of: http://identifiers.org/hgnc/30664
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2344
  bin: 9.25e1
  variant carriers: 0
hgvs: c.12-4G>A
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

11-72013422-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013422
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013422
    reference: chr 11
allele count: 20
allele frequency: 1.649919978881024e-4
allele num: 121218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.12-5C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.224+16G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.546-30C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1036-30C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1123-30C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.610-30C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1228-30C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1123-30C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1213-30C>T
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1078-30C>T
  variant of: http://identifiers.org/hgnc/30664
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15479
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6941
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20980
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 9178
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
hgvs: c.12-5C>T
num of homozygotes: 1
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD

11-72013433-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013433
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013433
    reference: chr 11
allele count: 365
allele frequency: 3.014735033698956e-3
allele num: 121072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1228-41C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1036-41C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.224+27G>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1213-41C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.12-16C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1123-41C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1078-41C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.546-41C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.610-41C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1123-41C>G
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 4.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 9.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 5.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 6.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 15329
  bin: 3.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 5.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 3.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20636
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 24068
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3734
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 4
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-72013434-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013434
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013434
    reference: chr 11
allele count: 1
allele frequency: 8.260093834665961e-6
allele num: 121064
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1213-42C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.224+28G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1123-42C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.610-42C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1123-42C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.12-17C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.546-42C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1078-42C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1228-42C>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1036-42C>G
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3740
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-72013442-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72013442
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72013442
    reference: chr 11
allele count: 1
allele frequency: 8.26541913940456e-6
allele num: 120986
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1228-50T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000255843
  ensembl transcript: ENST00000546065
  gene symbol: AP000593.7
  hgvsc: ENST00000546065.1:n.224+36A>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1213-50T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1123-50T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1123-50T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.546-50T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.610-50T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1078-50T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.12-25T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1036-50T>G
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6832
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23032
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-72018208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72018208
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72018208
    reference: chr 11
allele count: 52
allele frequency: 4.286326618088298e-4
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1077+35G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.609+35G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1122+35G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.545+35G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1227+35G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1035+35G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1122+35G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.11+35G>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1212+35G>A
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11214
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9725
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8886
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7649
  bin: 4.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 4791
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26021
  bin: 9.75e1
  variant carriers: 52
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

11-72018217-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72018217
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72018217
    reference: chr 11
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1212+26C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1122+26C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1227+26C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.11+26C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1035+26C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1122+26C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.609+26C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.545+26C>A
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1077+26C>A
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3962
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-72018227-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72018227
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72018227
    reference: chr 11
allele count: 5
allele frequency: 4.120313143798929e-5
allele num: 121350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1122+16T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.609+16T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.545+16T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1035+16T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1212+16T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1122+16T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.11+16T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1227+16T>G
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1077+16T>G
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9722
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2548
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5473
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

11-72018227-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72018227
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72018227
    reference: chr 11
allele count: 165
allele frequency: 1.359703337453646e-3
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000294053
  ensembl transcript: ENST00000294053
  gene symbol: CLPB
  hgvsc: ENST00000294053.3:c.1212+16T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000440423
  ensembl transcript: ENST00000535477
  gene symbol: CLPB
  hgvsc: ENST00000535477.1:c.1122+16T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000407296
  ensembl transcript: ENST00000437826
  gene symbol: CLPB
  hgvsc: ENST00000437826.2:c.1077+16T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000441518
  ensembl transcript: ENST00000538039
  gene symbol: CLPB
  hgvsc: ENST00000538039.1:c.1122+16T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000438372
  ensembl transcript: ENST00000544382
  gene symbol: CLPB
  hgvsc: ENST00000544382.1:c.545+16T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000443822
  ensembl transcript: ENST00000535990
  gene symbol: CLPB
  hgvsc: ENST00000535990.1:c.1227+16T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000340385
  ensembl transcript: ENST00000340729
  gene symbol: CLPB
  hgvsc: ENST00000340729.5:c.1035+16T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000445180
  ensembl transcript: ENST00000538021
  gene symbol: CLPB
  hgvsc: ENST00000538021.1:c.11+16T>C
  variant of: http://identifiers.org/hgnc/30664
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162129
  ensembl protein: ENSP00000439746
  ensembl transcript: ENST00000543042
  gene symbol: CLPB
  hgvsc: ENST00000543042.1:c.609+16T>C
  variant of: http://identifiers.org/hgnc/30664
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 4.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 11230
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7640
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 9722
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 9.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9025
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 7.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4662
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-72018232-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72018232
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72018232
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 29310
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 83
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3525
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3714
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6353
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65374
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.272727272727273e-5
allele num: 13750
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.812e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

FS
type: SiteQuality
SIO_000300: 1.5353e1

VQSLOD
type: SiteQuality
SIO_000300: -1.763e0

MQ
type: SiteQuality
SIO_000300: 5.453e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

QD
type: SiteQuality
SIO_000300: 9.07e0

DP
type: SiteQuality
SIO_000300: 2.532696e6

GenotypeQuality
all individuals: 479
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2156
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3712
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1958
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3767
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6393
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.25268349289237e-5
allele num: 13788
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.557e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.02e-1

FS
type: SiteQuality
SIO_000300: 1.2103e1

MQ
type: SiteQuality
SIO_000300: 5.444e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.858e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.119e0

QD
type: SiteQuality
SIO_000300: 1.5e0

DP
type: SiteQuality
SIO_000300: 2.533007e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

GenotypeQuality
all individuals: 822
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29310
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3496
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3714
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6402
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3768
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1142
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65386
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13790
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.064e0

MQRankSum
type: SiteQuality
SIO_000300: -2.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.63e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

VQSLOD
type: SiteQuality
SIO_000300: -2.471e0

QD
type: SiteQuality
SIO_000300: 1.103e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

DP
type: SiteQuality
SIO_000300: 2.533142e6

GenotypeQuality
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1913
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2156
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6658
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3508
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3711
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3769
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1969
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529005229197884e-5
allele num: 65402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13856
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 7.484e0

QD
type: SiteQuality
SIO_000300: 1.169e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 2.535478e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.986e0

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

GenotypeQuality
all individuals: 1976
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3549
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7050
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 799
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3715
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3769
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29306
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527977263698316e-5
allele num: 65446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13974
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.035e1

MQRankSum
type: SiteQuality
SIO_000300: 9.28e-1

DP
type: SiteQuality
SIO_000300: 2.541221e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

QD
type: SiteQuality
SIO_000300: 1.138e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

GenotypeQuality
all individuals: 86
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1895
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7188
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3528
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29305
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1975
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3771
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13986
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527370478983382e-5
allele num: 65472
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.3e-1

QD
type: SiteQuality
SIO_000300: 1.109e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.201e0

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

DP
type: SiteQuality
SIO_000300: 2.542382e6

FS
type: SiteQuality
SIO_000300: 2.599e0

MQ
type: SiteQuality
SIO_000300: 5.937e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.548e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

GenotypeQuality
all individuals: 3532
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29306
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3718
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3771
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526857422053929e-5
allele num: 65494
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14038
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.87e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 2.543119e6

QD
type: SiteQuality
SIO_000300: 1.169e1

FS
type: SiteQuality
SIO_000300: 2.016e0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.802e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.92e-1

GenotypeQuality
all individuals: 202
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29309
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 211
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3727
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1835
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3607
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524576167825345e-5
allele num: 65592
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.068e1

FS
type: SiteQuality
SIO_000300: 5.28e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.25e0

DP
type: SiteQuality
SIO_000300: 2.548529e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.15e-1

GenotypeQuality
all individuals: 714
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.049152335650689e-5
allele num: 65592
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
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East Asian
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allele frequency: 0.0e0
allele num: 8628
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South Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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BaseQRankSum
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DP
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MQ
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FS
type: SiteQuality
SIO_000300: 5.28e-1

ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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ClippingRankSum
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SIO_000300: -7.09e-1

GenotypeQuality
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variant carriers: 0

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

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.098304671301378e-5
allele num: 65592
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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MQ
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SIO_000300: 5.98e1

ReadPosRankSum
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SIO_000300: 5.15e-1

VQSLOD
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QD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.09e-1

FS
type: SiteQuality
SIO_000300: 5.28e-1

DP
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SIO_000300: 2.548529e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 870
num of homozygotes: 0

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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allele frequency: 0.0e0
allele num: 65670
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East Asian
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allele frequency: 0.0e0
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African
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allele count: 1
allele frequency: 9.689922480620155e-5
allele num: 10320
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 14348
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

DP
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MQRankSum
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BaseQRankSum
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SIO_000300: -1.094e0

InbreedingCoeff
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SIO_000300: 3.8e-3

VQSLOD
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FS
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SIO_000300: 0.0e0

QD
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ReadPosRankSum
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SIO_000300: 1.79e0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.548073133015979e-5
allele num: 65962
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.546e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

FS
type: SiteQuality
SIO_000300: 5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

DP
type: SiteQuality
SIO_000300: 2.571595e6

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

MQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

QD
type: SiteQuality
SIO_000300: 1.115e1

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

South Asian
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allele count: 1
allele frequency: 6.474168069403081e-5
allele num: 15446
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66138
num of homozygotes: 0

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

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

East Asian
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allele count: 0
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VQSLOD
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 1.366e0

ReadPosRankSum
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InbreedingCoeff
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QD
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MQ
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 7.51e-1

DP
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GenotypeQuality
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variant carriers: 0

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

Latino
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele num: 10392
num of homozygotes: 0

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

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

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

Latino
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num of homozygotes: 0

South Asian
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allele frequency: 6.206554121151936e-5
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African
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Other
type: Population
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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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QD
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FS
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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Latino
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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VQSLOD
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QD
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MQ
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500915558490679e-5
allele num: 66626
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -6.7e-2

DP
type: SiteQuality
SIO_000300: 2.603727e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.002e0

VQSLOD
type: SiteQuality
SIO_000300: 3.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e-1

FS
type: SiteQuality
SIO_000300: 5.47e-1

MQ
type: SiteQuality
SIO_000300: 5.99e1

QD
type: SiteQuality
SIO_000300: 1.524e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.244e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -3.609e0

InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 5.518e0

DP
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QD
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ReadPosRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.83e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

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

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

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.497e0

InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.92e-1

FS
type: SiteQuality
SIO_000300: 5.623e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.264e0

ReadPosRankSum
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SIO_000300: 1.03e0

DP
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SIO_000300: 2.603646e6

MQRankSum
type: SiteQuality
SIO_000300: -3.93e-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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variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.3963e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-2

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: -2.144e0

QD
type: SiteQuality
SIO_000300: 1.28e1

DP
type: SiteQuality
SIO_000300: 2.603573e6

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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variant carriers: 28

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 3
allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 3.601116346067281e-4
allele num: 66646
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.466e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 5.49e0

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.972e1

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

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

South Asian
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allele frequency: 2.42306760358614e-4
allele num: 16508
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

East Asian
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allele count: 0
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Latino
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African
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allele frequency: 9.611687812379854e-5
allele num: 10404
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South Asian
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Other
type: Population
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MQ
type: SiteQuality
SIO_000300: 5.829e1

MQRankSum
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VQSLOD
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FS
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QD
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11578
num of homozygotes: 0

European (Finnish)
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South Asian
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allele num: 16512
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Other
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African
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allele frequency: 3.94079200307574e-3
allele num: 10404
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.998320940273447e-5
allele num: 66704
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East Asian
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FS
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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MQ
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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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European (Non-Finnish)
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African
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East Asian
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Latino
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South Asian
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European (Finnish)
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Other
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DP
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MQ
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ClippingRankSum
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MQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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QD
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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BaseQRankSum
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FS
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VQSLOD
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MQ
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DP
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ReadPosRankSum
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QD
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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South Asian
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African
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European (Non-Finnish)
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Other
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Latino
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MQRankSum
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ReadPosRankSum
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FS
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DP
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VQSLOD
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QD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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East Asian
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ClippingRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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African
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Other
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Latino
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European (Non-Finnish)
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VQSLOD
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BaseQRankSum
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FS
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MQ
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MQRankSum
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ClippingRankSum
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QD
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DP
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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South Asian
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African
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European (Non-Finnish)
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Latino
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQ
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MQRankSum
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FS
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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Other
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South Asian
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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Latino
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European (Finnish)
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South Asian
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East Asian
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European (Non-Finnish)
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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QD
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DP
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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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variant carriers: 0

GenotypeQuality
all individuals: 3818
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3579
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3732
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004717406327935e-5
allele num: 66562
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16168
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.911e0

DP
type: SiteQuality
SIO_000300: 2.579844e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

MQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.95e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.327e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.38e0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3678
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3727
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15630
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506977304921788e-5
allele num: 66358
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.439e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.034e0

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

DP
type: SiteQuality
SIO_000300: 2.560639e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 9.097e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.025e0

VQSLOD
type: SiteQuality
SIO_000300: -1.014e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.82e-1

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3728
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508022680661117e-5
allele num: 66312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15560
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.869e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.92e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.163e0

VQSLOD
type: SiteQuality
SIO_000300: -1.481e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

QD
type: SiteQuality
SIO_000300: 9.960000000000001e0

DP
type: SiteQuality
SIO_000300: 2.557458e6

GenotypeQuality
all individuals: 2166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3777
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29221
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3518
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3723
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3485
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65958
num of homozygotes: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.930874686232864e-4
allele num: 10358
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.327e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

DP
type: SiteQuality
SIO_000300: 2.51828e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.14e-1

MQ
type: SiteQuality
SIO_000300: 5.132e1

MQRankSum
type: SiteQuality
SIO_000300: -4.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 5.19e0

GenotypeQuality
all individuals: 113
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3502
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
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variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 283
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variant carriers: 0

GenotypeQuality
all individuals: 3722
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29220
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3401
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.724045185583647e-5
allele num: 14872
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 2.512802e6

VQSLOD
type: SiteQuality
SIO_000300: 2.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQRankSum
type: SiteQuality
SIO_000300: -7.73e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.85e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

FS
type: SiteQuality
SIO_000300: 6.368e0

GenotypeQuality
all individuals: 139
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2302
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6093
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1934
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variant carriers: 0

GenotypeQuality
all individuals: 3718
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3775
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
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variant carriers: 0

GenotypeQuality
all individuals: 3290
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variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 2.886046723577483e-4
allele num: 65834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14750
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.667440061871617e-5
allele num: 10344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.945e1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

DP
type: SiteQuality
SIO_000300: 2.50617e6

QD
type: SiteQuality
SIO_000300: 1.594e1

FS
type: SiteQuality
SIO_000300: 8.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22096
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variant carriers: 0

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

GenotypeQuality
all individuals: 206
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 610
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variant carriers: 0

GenotypeQuality
all individuals: 1759
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variant carriers: 0

GenotypeQuality
all individuals: 3848
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
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variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3777
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9174
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.18e0

QD
type: SiteQuality
SIO_000300: 1.744e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

DP
type: SiteQuality
SIO_000300: 2.056736e6

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.25e1
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GenotypeQuality
all individuals: 9906
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 1699
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GenotypeQuality
all individuals: 9198
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variant carriers: 0

GenotypeQuality
all individuals: 2347
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variant carriers: 0

GenotypeQuality
all individuals: 159
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 24437
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.646922631680494e-5
allele num: 10366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.939e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 6.741e0

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.94e0

QD
type: SiteQuality
SIO_000300: 1.207e1

MQRankSum
type: SiteQuality
SIO_000300: -7.64e-1

DP
type: SiteQuality
SIO_000300: 2.064214e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.91e-1

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4915
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24461
bin: 6.25e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.064476e6

QD
type: SiteQuality
SIO_000300: 3.81e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.96e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.874e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: -9.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.23e-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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bin: 8.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.505028369007235e-5
allele num: 66622
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

FS
type: SiteQuality
SIO_000300: 4.085e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.39e-1

QD
type: SiteQuality
SIO_000300: 1.541e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

VQSLOD
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SIO_000300: 1.96e0

DP
type: SiteQuality
SIO_000300: 2.065624e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.1605e1

VQSLOD
type: SiteQuality
SIO_000300: -1.72e0

DP
type: SiteQuality
SIO_000300: 2.06786e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.31e0

QD
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SIO_000300: 1.014e1

MQRankSum
type: SiteQuality
SIO_000300: 7.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.258e0

MQ
type: SiteQuality
SIO_000300: 5.826e1

GenotypeQuality
all individuals: 9209
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 7.011e0

VQSLOD
type: SiteQuality
SIO_000300: -7.514e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 2.068533e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.303e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.062e0

GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.646922631680494e-5
allele num: 10366
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.068901e6

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.983e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 1.4129e1

VQSLOD
type: SiteQuality
SIO_000300: -1.736e0

QD
type: SiteQuality
SIO_000300: 1.207e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.131e0

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 4
allele frequency: 3.458412588621823e-4
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.499925003749812e-4
allele num: 66670
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.241910071506484e-4
allele num: 16502
num of homozygotes: 0

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

Other
type: Population
allele count: 2
allele frequency: 2.207505518763797e-3
allele num: 906
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.01e-1

InbreedingCoeff
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-2

FS
type: SiteQuality
SIO_000300: 5.47e-1

DP
type: SiteQuality
SIO_000300: 2.070399e6

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
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QD
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VQSLOD
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BaseQRankSum
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
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FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.499370088187654e-5
allele num: 66676
num of homozygotes: 0

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

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

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

African
type: Population
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Other
type: Population
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allele num: 906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.93e-1

InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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MQ
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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BaseQRankSum
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SIO_000300: 3.22e0

MQRankSum
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SIO_000300: 4.36e-1

ReadPosRankSum
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SIO_000300: 7.68e-1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.64e0

QD
type: SiteQuality
SIO_000300: 1.593e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.070663e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.637625289128758e-5
allele num: 10376
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 6
allele frequency: 8.99685110211426e-5
allele num: 66690
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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MQ
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SIO_000300: 5.976e1

VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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MQRankSum
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SIO_000300: 6.15e-1

QD
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SIO_000300: 1.247e1

FS
type: SiteQuality
SIO_000300: 1.101e0

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
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allele count: 27
allele frequency: 1.636363636363636e-3
allele num: 16500
num of homozygotes: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

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

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

DP
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SIO_000300: 2.072988e6

MQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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BaseQRankSum
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QD
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FS
type: SiteQuality
SIO_000300: 1.107e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeQuality
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variant carriers: 21

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 21
allele frequency: 3.148992322456814e-4
allele num: 66688
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.107e0

QD
type: SiteQuality
SIO_000300: 1.16e1

MQRankSum
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SIO_000300: 1.95e-1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

DP
type: SiteQuality
SIO_000300: 2.072988e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.96e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.88e0

GenotypeDepth
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

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

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

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

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

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

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

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

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

Other
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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

South Asian
type: Population
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allele frequency: 6.06060606060606e-5
allele num: 16500
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 frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

South Asian
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allele frequency: 6.06060606060606e-5
allele num: 16500
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

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

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2318
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3562
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 2.353e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.525e0

VQSLOD
type: SiteQuality
SIO_000300: 9.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.38e-1

DP
type: SiteQuality
SIO_000300: 2.032602e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.123e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4674
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 3.748912815283568e-4
allele num: 66686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 27
allele frequency: 4.082249773208346e-3
allele num: 6614
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.805618e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.117e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.13e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.324e1

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5472
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.178e1

DP
type: SiteQuality
SIO_000300: 2.807102e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.564e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.768e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.153e0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

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: 3954
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.496251874062968e-5
allele num: 66700
num of homozygotes: 0

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 5.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

MQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

QD
type: SiteQuality
SIO_000300: 1.293e1

DP
type: SiteQuality
SIO_000300: 2.81233e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.21e-2

MQ
type: SiteQuality
SIO_000300: 5.988e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.77e-1

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

GenotypeQuality
all individuals: 9994
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 164

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5473
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 5
allele frequency: 4.323015735777278e-4
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 6.662628709872804e-4
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.535833081342606e-4
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 134
allele frequency: 2.008995502248876e-3
allele num: 66700
num of homozygotes: 1

African
type: Population
allele count: 6
allele frequency: 5.767012687427913e-4
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 6.607929515418502e-3
allele num: 908
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.293e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

DP
type: SiteQuality
SIO_000300: 2.81233e6

MQ
type: SiteQuality
SIO_000300: 5.988e1

MQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

FS
type: SiteQuality
SIO_000300: 5.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.21e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.77e-1